AR111629A1 - Mezclas fungicidas que comprenden 3-fenil-5-(trifluorometil)-1,2,4-oxadiazoles - Google Patents
Mezclas fungicidas que comprenden 3-fenil-5-(trifluorometil)-1,2,4-oxadiazolesInfo
- Publication number
- AR111629A1 AR111629A1 ARP180101112A ARP180101112A AR111629A1 AR 111629 A1 AR111629 A1 AR 111629A1 AR P180101112 A ARP180101112 A AR P180101112A AR P180101112 A ARP180101112 A AR P180101112A AR 111629 A1 AR111629 A1 AR 111629A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- phenyl
- ethyl
- inhibitors
- pyrazol
- Prior art date
Links
- 239000000417 fungicide Substances 0.000 title abstract 3
- 230000000855 fungicidal effect Effects 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 25
- -1 C3−8-cycloalkenyl Chemical group 0.000 abstract 24
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 abstract 11
- 230000015572 biosynthetic process Effects 0.000 abstract 9
- 150000003839 salts Chemical class 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 239000002253 acid Substances 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- 150000004702 methyl esters Chemical class 0.000 abstract 4
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 4
- 238000003786 synthesis reaction Methods 0.000 abstract 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- NWBJYWHLCVSVIJ-UHFFFAOYSA-N N-benzyladenine Chemical compound N=1C=NC=2NC=NC=2C=1NCC1=CC=CC=C1 NWBJYWHLCVSVIJ-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 3
- 150000003254 radicals Chemical class 0.000 abstract 3
- 239000011734 sodium Substances 0.000 abstract 3
- 229910052708 sodium Inorganic materials 0.000 abstract 3
- JLIDBLDQVAYHNE-YKALOCIXSA-N (+)-Abscisic acid Chemical compound OC(=O)/C=C(/C)\C=C\[C@@]1(O)C(C)=CC(=O)CC1(C)C JLIDBLDQVAYHNE-YKALOCIXSA-N 0.000 abstract 2
- YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 abstract 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 2
- 239000005630 Diquat Substances 0.000 abstract 2
- 102000015782 Electron Transport Complex III Human genes 0.000 abstract 2
- 108010024882 Electron Transport Complex III Proteins 0.000 abstract 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 abstract 2
- 150000001204 N-oxides Chemical class 0.000 abstract 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 abstract 2
- 229930182558 Sterol Natural products 0.000 abstract 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 abstract 2
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 abstract 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 230000032823 cell division Effects 0.000 abstract 2
- MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 abstract 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 abstract 2
- XPEVJXBWHXAUDR-UHFFFAOYSA-N epyrifenacil Chemical compound CCOC(=O)COC1=NC=CC=C1OC1=CC(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)=C(F)C=C1Cl XPEVJXBWHXAUDR-UHFFFAOYSA-N 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 abstract 2
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 abstract 2
- 150000002632 lipids Chemical class 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 abstract 2
- 150000003904 phospholipids Chemical class 0.000 abstract 2
- 239000012268 protein inhibitor Substances 0.000 abstract 2
- 229940121649 protein inhibitor Drugs 0.000 abstract 2
- 230000029058 respiratory gaseous exchange Effects 0.000 abstract 2
- 150000003432 sterols Chemical class 0.000 abstract 2
- 235000003702 sterols Nutrition 0.000 abstract 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 abstract 2
- QFNFRZHOXWNWAQ-UHFFFAOYSA-N triclopyricarb Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NC(Cl)=C(Cl)C=C1Cl QFNFRZHOXWNWAQ-UHFFFAOYSA-N 0.000 abstract 2
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 abstract 1
- UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 abstract 1
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 abstract 1
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 abstract 1
- CXNPLSGKWMLZPZ-GIFSMMMISA-N (2r,3r,6s)-3-[[(3s)-3-amino-5-[carbamimidoyl(methyl)amino]pentanoyl]amino]-6-(4-amino-2-oxopyrimidin-1-yl)-3,6-dihydro-2h-pyran-2-carboxylic acid Chemical compound O1[C@@H](C(O)=O)[C@H](NC(=O)C[C@@H](N)CCN(C)C(N)=N)C=C[C@H]1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-GIFSMMMISA-N 0.000 abstract 1
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 abstract 1
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 abstract 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- ADDQHLREJDZPMT-AWEZNQCLSA-N (S)-metamifop Chemical compound O=C([C@@H](OC=1C=CC(OC=2OC3=CC(Cl)=CC=C3N=2)=CC=1)C)N(C)C1=CC=CC=C1F ADDQHLREJDZPMT-AWEZNQCLSA-N 0.000 abstract 1
- RMOGWMIKYWRTKW-UONOGXRCSA-N (S,S)-paclobutrazol Chemical compound C([C@@H]([C@@H](O)C(C)(C)C)N1N=CN=C1)C1=CC=C(Cl)C=C1 RMOGWMIKYWRTKW-UONOGXRCSA-N 0.000 abstract 1
- DARPYRSDRJYGIF-PTNGSMBKSA-N (Z)-3-ethoxy-2-naphthalen-2-ylsulfonylprop-2-enenitrile Chemical compound C1=CC=CC2=CC(S(=O)(=O)C(\C#N)=C/OCC)=CC=C21 DARPYRSDRJYGIF-PTNGSMBKSA-N 0.000 abstract 1
- OVXMBIVWNJDDSM-UHFFFAOYSA-N (benzhydrylideneamino) 2,6-bis[(4,6-dimethoxypyrimidin-2-yl)oxy]benzoate Chemical compound COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C(=O)ON=C(C=2C=CC=CC=2)C=2C=CC=CC=2)=N1 OVXMBIVWNJDDSM-UHFFFAOYSA-N 0.000 abstract 1
- CKPCAYZTYMHQEX-NBVRZTHBSA-N (e)-1-(2,4-dichlorophenyl)-n-methoxy-2-pyridin-3-ylethanimine Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=N/OC)/CC1=CC=CN=C1 CKPCAYZTYMHQEX-NBVRZTHBSA-N 0.000 abstract 1
- MQTJFBGZJVKRDO-HJWRWDBZSA-N (z)-3-amino-2-cyano-3-phenylprop-2-enoic acid Chemical compound N#C/C(C(O)=O)=C(/N)C1=CC=CC=C1 MQTJFBGZJVKRDO-HJWRWDBZSA-N 0.000 abstract 1
- XBCKTJDKWPZLJH-ZUPCBTBPSA-N (z,2e)-5-[1-(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-n,3-dimethylpent-3-enamide Chemical compound N1=C(OC\C=C(\C)/C(=N\OC)/C(=O)NC)C=CN1C1=CC=C(Cl)C=C1 XBCKTJDKWPZLJH-ZUPCBTBPSA-N 0.000 abstract 1
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 abstract 1
- PYCINWWWERDNKE-UHFFFAOYSA-N 1-(2-chloro-6-propylimidazo[1,2-b]pyridazin-3-yl)sulfonyl-3-(4,6-dimethoxypyrimidin-2-yl)urea Chemical compound N12N=C(CCC)C=CC2=NC(Cl)=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 PYCINWWWERDNKE-UHFFFAOYSA-N 0.000 abstract 1
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 abstract 1
- VQHHIQJPQOLZGF-UHFFFAOYSA-N 1-(2-iodophenyl)sulfonyl-3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)I)=N1 VQHHIQJPQOLZGF-UHFFFAOYSA-N 0.000 abstract 1
- RBSXHDIPCIWOMG-UHFFFAOYSA-N 1-(4,6-dimethoxypyrimidin-2-yl)-3-(2-ethylsulfonylimidazo[1,2-a]pyridin-3-yl)sulfonylurea Chemical compound CCS(=O)(=O)C=1N=C2C=CC=CN2C=1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 RBSXHDIPCIWOMG-UHFFFAOYSA-N 0.000 abstract 1
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 abstract 1
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 abstract 1
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 abstract 1
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 abstract 1
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 abstract 1
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 abstract 1
- CCZNNOPONAPVCR-UHFFFAOYSA-N 1-[3-bromo-2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]phenyl]-4-methyltetrazol-5-one Chemical compound O=C1N(C)N=NN1C1=CC=CC(Br)=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 CCZNNOPONAPVCR-UHFFFAOYSA-N 0.000 abstract 1
- NVASWJQSCINQCX-UHFFFAOYSA-N 1-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-cyclopropyl-2-(1,2,4-triazol-1-yl)ethanol Chemical compound C1CC1C(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)C(F)(F)F)(O)CN1C=NC=N1 NVASWJQSCINQCX-UHFFFAOYSA-N 0.000 abstract 1
- IXWKBUKANTXHJH-UHFFFAOYSA-N 1-[5-chloro-2-methyl-4-(5-methyl-5,6-dihydro-1,4,2-dioxazin-3-yl)pyrazol-3-yl]sulfonyl-3-(4,6-dimethoxypyrimidin-2-yl)urea Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=C(Cl)C=2C=2OC(C)CON=2)C)=N1 IXWKBUKANTXHJH-UHFFFAOYSA-N 0.000 abstract 1
- HILAYQUKKYWPJW-UHFFFAOYSA-N 1-dodecylguanidine Chemical compound CCCCCCCCCCCCN=C(N)N HILAYQUKKYWPJW-UHFFFAOYSA-N 0.000 abstract 1
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 abstract 1
- QDKWLJJOYIFEBS-UHFFFAOYSA-N 1-fluoro-4-$l^{1}-oxidanylbenzene Chemical group [O]C1=CC=C(F)C=C1 QDKWLJJOYIFEBS-UHFFFAOYSA-N 0.000 abstract 1
- BXKKQFGRMSOANI-UHFFFAOYSA-N 1-methoxy-3-[4-[(2-methoxy-2,4,4-trimethyl-3h-chromen-7-yl)oxy]phenyl]-1-methylurea Chemical compound C1=CC(NC(=O)N(C)OC)=CC=C1OC1=CC=C2C(C)(C)CC(C)(OC)OC2=C1 BXKKQFGRMSOANI-UHFFFAOYSA-N 0.000 abstract 1
- WXJYKXOIFICRPR-UHFFFAOYSA-L 1-methyl-4-(1-methylpyridin-1-ium-4-yl)pyridin-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.COS([O-])(=O)=O.C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 WXJYKXOIFICRPR-UHFFFAOYSA-L 0.000 abstract 1
- VHVCMKPRANXWKQ-UHFFFAOYSA-N 1-methyl-4-[3-methyl-2-[[2-methyl-4-(1-methylpyrazol-3-yl)phenoxy]methyl]phenyl]tetrazol-5-one Chemical compound CN1N=NN(C1=O)C1=C(C(=CC=C1)C)COC1=C(C=C(C=C1)C1=NN(C=C1)C)C VHVCMKPRANXWKQ-UHFFFAOYSA-N 0.000 abstract 1
- PRPINYUDVPFIRX-UHFFFAOYSA-N 1-naphthaleneacetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CC=CC2=C1 PRPINYUDVPFIRX-UHFFFAOYSA-N 0.000 abstract 1
- KNGWEAQJZJKFLI-UHFFFAOYSA-N 2,2-dimethyl-4h-1,3-benzodioxine-6-carbaldehyde Chemical compound O=CC1=CC=C2OC(C)(C)OCC2=C1 KNGWEAQJZJKFLI-UHFFFAOYSA-N 0.000 abstract 1
- ZMZGFLUUZLELNE-UHFFFAOYSA-N 2,3,5-triiodobenzoic acid Chemical compound OC(=O)C1=CC(I)=CC(I)=C1I ZMZGFLUUZLELNE-UHFFFAOYSA-N 0.000 abstract 1
- DFPIGVDNBRPLIL-UHFFFAOYSA-N 2,3-dimethyl-5-(4-methylphenyl)-3-pyridin-3-yl-1,2-oxazolidine Chemical compound CN1OC(C=2C=CC(C)=CC=2)CC1(C)C1=CC=CN=C1 DFPIGVDNBRPLIL-UHFFFAOYSA-N 0.000 abstract 1
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 abstract 1
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 abstract 1
- DNBMPXLFKQCOBV-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OCCOCCOCC)=NC2=C1 DNBMPXLFKQCOBV-UHFFFAOYSA-N 0.000 abstract 1
- SCFZORZKZIEAIV-UHFFFAOYSA-N 2-(3-ethynyl-8-methylquinolin-6-yl)oxy-2-methoxy-n-propylacetamide Chemical compound N1=CC(C#C)=CC2=CC(OC(OC)C(=O)NCCC)=CC(C)=C21 SCFZORZKZIEAIV-UHFFFAOYSA-N 0.000 abstract 1
- ZZXLGPONYSOLKU-UHFFFAOYSA-N 2-(3-ethynyl-8-methylquinolin-6-yl)oxy-2-methylsulfanyl-n-propylacetamide Chemical compound N1=CC(C#C)=CC2=CC(OC(C(=O)NCCC)SC)=CC(C)=C21 ZZXLGPONYSOLKU-UHFFFAOYSA-N 0.000 abstract 1
- LQIVUKUXIHENQE-UHFFFAOYSA-N 2-(3-ethynyl-8-methylquinolin-6-yl)oxy-n-(2-fluoroethyl)-2-methoxyacetamide Chemical compound N1=CC(C#C)=CC2=CC(OC(OC)C(=O)NCCF)=CC(C)=C21 LQIVUKUXIHENQE-UHFFFAOYSA-N 0.000 abstract 1
- FTROJHYITVGKDZ-UHFFFAOYSA-N 2-(3-ethynyl-8-methylquinolin-6-yl)oxy-n-(2-fluoroethyl)-2-methylsulfanylacetamide Chemical compound N1=CC(C#C)=CC2=CC(OC(SC)C(=O)NCCF)=CC(C)=C21 FTROJHYITVGKDZ-UHFFFAOYSA-N 0.000 abstract 1
- OMKJEAMIPWDWAL-UHFFFAOYSA-N 2-(3-ethynyl-8-methylquinolin-6-yl)oxy-n-propylbutanamide Chemical compound N1=CC(C#C)=CC2=CC(OC(CC)C(=O)NCCC)=CC(C)=C21 OMKJEAMIPWDWAL-UHFFFAOYSA-N 0.000 abstract 1
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 abstract 1
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 abstract 1
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- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 abstract 1
- AZHZOGYUMMIAOF-UHFFFAOYSA-N trifludimoxazin Chemical compound O=C1N(C)C(=S)N(C)C(=O)N1C(C(=C1)F)=CC2=C1OC(F)(F)C(=O)N2CC#C AZHZOGYUMMIAOF-UHFFFAOYSA-N 0.000 abstract 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 abstract 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 abstract 1
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 abstract 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 abstract 1
- RVKCCVTVZORVGD-UHFFFAOYSA-N trinexapac-ethyl Chemical group O=C1CC(C(=O)OCC)CC(=O)C1=C(O)C1CC1 RVKCCVTVZORVGD-UHFFFAOYSA-N 0.000 abstract 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 abstract 1
- 239000003744 tubulin modulator Substances 0.000 abstract 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 abstract 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 abstract 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 abstract 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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- Plural Heterocyclic Compounds (AREA)
Abstract
Reivindicación 1: Una mezcla fungicida caracterizada porque comprende como componentes activos 1) al menos un compuesto activo de la fórmula (1), o un N-óxido, o una sal de aquel aceptable en la agricultura, en donde: W es -(C=O)-NR²-#, -(C=S)-NR²-#, -NR²-(C=O)-# o -NR²-(C=S)-#; en donde # indica la posición, que está unida al grupo R¹; R¹ es C₁₋₆-alquilo, C₃₋₈-cicloalquilo, C₃₋₈-cicloalquenilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxiimino-C₁₋₄-alquilo o fenilo; en donde el anillo de fenilo es no sustituido o sustituido con 1, 2, 3 o hasta la cantidad máxima posible de radicales idénticos o diferentes seleccionados del grupo que consiste en halógeno, C₁₋₆-alquilo y C₁₋₆-alcoxi; R² es hidrógeno, C₁₋₆-alquilo, C₂₋₆-alquenilo, C₂₋₆-alquinilo, C₁₋₆-alcoxi, C₃₋₈-cicloalquilo, C₃₋₈-cicloalquenilo y C₃₋₈- cicloalquil-C₁₋₄-alquilo; y en donde cualquiera de los grupos alifáticos o cíclicos es no sustituido o sustituido con 1, 2, 3 o hasta la máxima cantidad posible de radicales idénticos o diferentes seleccionados del grupo que consiste en halógeno, hidroxi, oxo, ciano, C₁₋₆alquilo, C₁₋₆alcoxi y C₃₋₈-cicloalquilo; o R¹ y R², junto con el átomo de nitrógeno al que están unidos, forman un heterociclo monocíclico o bicíclico saturado o parcialmente insaturado de 3 a 7 miembros, en donde el heterociclo incluye, además de un átomo de nitrógeno -y uno- o más átomos de carbono, ningún heteroátomo adicional o 1, 2 ó 3 heteroátomos adicionales seleccionados independientemente de N, O y S como átomos miembros del anillo; y en donde uno o dos grupos CH₂ del heterociclo se pueden reemplazar por uno o dos grupos seleccionados independientemente del grupo de -C(=O)- y -C(=S)-; y en donde el heterociclo es no sustituido o tiene 1, 2, 3, y 4 o hasta la máxima cantidad posible de radicales idénticos o diferentes seleccionados del grupo que consiste en halógeno, ciano, C₁₋₆-alquilo, C₁₋₆-alquilo, C₁₋₆-haloalquilo, C₁₋₆-alcoxi, m es 0 ó 1; R³, R⁴ se seleccionan, independientemente entre sí, del grupo que consiste en hidrógeno, halógeno, ciano, C₁₋₄-alquilo, C₁₋₄-alquenilo, C₁₋₄-alquinilo, C₁₋₄-haloalquilo y C₁₋₄-alcoxi; o R³ y R⁴, junto con el átomo de carbono al que están unidos, forman un anillo de ciclopropilo; y como componente 2) al menos un compuesto activo II seleccionado de los grupos A) a O), o un N-óxido, o una sal de aquel aceptable en la agricultura: A) Inhibidores de la respiración: Inhibidores del complejo III en el sitio Qₒ: azoxistrobina (A.1.1), coumetoxistrobina (A.1.2), coumoxistrobina (A.1.3), dimoxistrobina (A.1.4), enestroburina (A.1.5), fenaminstrobina (A.1.6), fenoxi-strobina / flufenoxistrobina (A.1.7), fluoxastrobina (A.1.8), cresoxim-metilo (A.1.9), mandestrobina (A.1.10), metominostrobina (A.1.11), orisastrobina (A.1.12), picoxistrobina (A.1.13), piraclostrobina (A.1.14), pirametostrobina (A.1.15), piraoxistrobina (A.1.16), trifloxistrobina (A.1.17), 2-(2-(3-(2,6-diclorofenil)-1-metil-alilidenaminooximetil)-fenil)-2-metoxiimino-N-metil-acetamida (A.1.18), piribencarb (A.1.19), triclopiricarb / clorodincarb (A.1.20), famoxadona (A.1.21), fenamidona (A.1.21), metil-N-[2-[(1,4-dimetil-5-fenil-pirazol-3-il)oxilmetil]fenil]-N-metoxi-carbamato (A.1.22), 1-[3-cloro-2-[[1-(4-clorofenil)-1H-pirazol-3-il]oximetil]fenil]-4-metil-tetrazol-5-ona (A.1.23), 1-[3-bromo-2-[[1-(4-clorofenil)pirazol-3-il]oximetil]fenil]-4-metil-tetrazol-5-ona (A.1.24), 1-[2-[[1-(4-clorofenil)pirazol-3-il]oximetil]-3-metil-fenil]-4-metil-tetrazol-5-ona (A.1.25), 1-[2-[[1-(4-clorofenil)pirazol-3-il]oximetil]-3-fluoro-fenil]-4-metil-tetrazol-5-ona (A.1.26), 1-[2-[[1-(2,4-diclorofenil)pirazol-3-il]oximetil]-3-fluoro-fenil]-4-metil-tetrazol-5-ona (A.1.27), 1-[2-[[4-(4-clorofenil)tiazol-2-il]oximetil]-3-metil-fenil]-4-metil-tetrazol-5-ona (A.1.28), 1-[3-cloro-2-[[4-(p-tolil)tiazol-2-il]oximetil]fenil]-4-metil-tetrazol-5-ona (A.1.29), 1-[3-ciclopropil-2-[[2-metil-4-(1-metilpirazol-3-il)fenoxi]metil]fenil]-4-metil-tetrazol-5-ona (A.1.30), 1-[3-(difluorometoxi)-2-[[2-metil-4-(1-metilpirazol-3-il)fenoxi]metil]fenil]-4-metil-tetrazol-5-ona (A.1.31), 1-metil-4-[3-metil-2-[[2-metil-4-(1-metilpirazol-3-il)fenoxi]metil]fenil]tetrazol-5-ona (A.1.32), 1-metil-4-[3-metil-2-[[1-[3-(trifluorometil)fenil]-etilidenamino]oximetil]fenil]-tetrazol-5-ona (A.1.33), (Z,2E)-5-[1-(2,4-diclorofenil)pirazol-3-il]-oxi-2-metoxiimino-N,3-dimetil-pent-3-enamida (A.1.34), (Z,2E)-5-[1-(4-clorofenil)pirazol-3-il]oxi-2-metoxiimino-N,3-dimetil-pent-3-enamida (A.1.35), piriminostrobina (A.1.36), bifujunzhi (A.1.37), metiléster del ácido 2-(orto-((2,5-dimetilfenil-oximetilen)fenil)-3-metoxi-acrílico (A.1.38); Inhibidores del complejo III en el sitio Qⁱ: ciazofamida (A.2.1), amisulbrom (A.2.2), 2-metilpropanoato de [(6S,7R,8R)-8-bencil-3-[(3-hidroxi-4-metoxi-piridin-2-carbonil)amino]-6-metil-4,9-dioxo-1,5-dioxonan-7-ilo] (A.2.3), fenpicoxamid (A.2.4), 2-metilpropanoato de [(6S,7R,8R)-8-bencil-3-[[4-metoxi-3-(propanoiloximetoxi)piridin-2-carbonil]amino]-6-metil-4,9-dioxo-1,5-dioxonan-7-ilo] (A.2.5), florilpicoxamid (A.2.6); Inhibidores del complejo II: benodanil (A.3.1), benzovindiflupir (A.3.2), bixafeno (A.3.3), boscalid (A.3.4), carboxín (A.3.5), fenfuram (A.3.6), fluopiram (A.3.7), flutolanil (A.3.8), fluxapiroxad (A.3.9), furametpir (A.3.10), isofetamida (A.3.11), isopirazam (A.3.12), mepronil (A.3.13), oxicarboxín (A.3.14), penflufen (A.3.15), pentiopirad (A.3.16), pidiflumetofeno (A.3.17), N-[2-(3,4-difluorofenil)fenil]-3-(trifluorometil)pirazin-2-carboxamida (A.3.18), sedaxano (A.3.19), tecloftalam (A.3.20), tifluzamida (A.3.21), 3-(difluorometil)-1-metil-N-(1,1,3-trimetilindan-4-il)pirazol-4-carboxamida (A.3.22), 3-(trifluorometil)-1-metil-N-(1,1,3-trimetilindan-4-il)pirazol-4-carboxamida (A.3.23), 1,3-di-metil-N-(1,1,3-trimetilindan-4-il)pirazol-4-carboxamida (A.3.24), 3-(trifluorometil)-1,5-dimetil-N-(1,1,3-trimetilindan-4-il)pirazol-4-carboxamida (A.3.25), 1,3,5-trimetil-N-(1,1,3-trimetilindan-4-il)pirazol-4-carboxamida (A.3.26), 3-(difluorometil)-1,5-dimetil-N-(1,1,3-trimetilindan-4-il)pirazol-4-carboxamida (A.3.27), 3-(difluorometil)-N-(7-fluoro-1,1,3-trimetil-indan-4-il)-1-metil-pirazol-4-carboxamida (A.3.28), N-[2-[2-cloro-4-(trifluorometil)fenoxi]fenil]-3-(difluorometil)-5-fluoro-1-metil-pirazol-4-carboxamida (A.3.29), metil (E)-2-[2-[(5-ciano-2-metil-fenoxi)metil]fenil]-3-metoxi-prop-2-enoato (A.3.30), N-[(5-cloro-2-isopropil-fenil)metil]-N-ciclopropil-3-(difluorometil)-5-fluoro-1-metil-pirazol-4-carboxamida (A.3.31), 2-(difluorometil)-N-(1,1,3-trimetil-indan-4-il)piridin-3-carboxamida (A.3.32), 2-(difluorometil)-N-[(3R)-1,1,3-trimetilindan-4-il]piridin-3-carboxamida (A.3.33), 2-(difluorometil)-N-(3-etil-1,1-dimetil-indan-4-il)piridin-3-carboxamida (A.3.34), 2-(difluorometil)-N-[(3R)-3-etil-1,1-dimetil-indan-4-il]piridin-3-carboxamida (A.3.35), 2-(difluorometil)-N-(1,1-dimetil-3-propil-indan-4-il)piridin-3-carboxamida (A.3.36), 2-(difluorometil)-N-[(3R)-1,1-dimetil-3-propil-indan-4-il]piridin-3-carboxamida (A.3.37), 2-(difluorometil)-N-(3-isobutil-1,1-dimetil-indan-4-il)piridin-3-carboxamida (A.3.38), 2-(difluorometil)-N-[(3R)-3-isobutil-1,1-dimetil-indan-4-il]piridin-3-carboxamida (A.3.39); Otros inhibidores de la respiración: diflumetorim (A.4.1); derivados de nitrofenilo: binapacrilo (A.4.2), dinobutón (A.4.3), dinocap (A.4.4), fluazinam (A.4.5), meptildinocap (A.4.6), ferimzona (A.4.7); compuestos de organometal: sales de fentín, por ejemplo, fentín-acetato (A.4.8), cloruro de fentín (A.4.9) o hidróxido de fentín (A.4.10); ametoctradin (A.4.11); siltiofam (A.4.12); B) Inhibidores de la biosíntesis del esterol (fungicidas de SBI): Inhibidores de C₁₄ desmetilasa: triazoles: azaconazol (B.1.1), bitertanol (B.1.2), bromuconazol (B.1.3), ciproconazol (B.1.4), difenoconazol (B.1.5), diniconazol (B.1.6), diniconazol-M (B.1.7), epoxiconazol (B.1.8), fenbuconazol (B.1.9), fluquinconazol (B.1.10), flusilazol (B.1.11), flutriafol (B.1.12), hexaconazol (B.1.13), imibenconazol (B.1.14), ipconazol (B.1.15), metconazol (B.1.17), miclobutanil (B.1.18), oxpoconazol (B.1.19), paclobutrazol (B.1.20), penconazol (B.1.21), propiconazol (B.1.22), protioconazol (B.1.23), simeconazol (B.1.24), tebuconazol (B.1.25), tetraconazol (B.1.26), triadimefón (B.1.27), triadimenol (B.1.28), triticonazol (B.1.29), uniconazol (B.1.30), 1-[rel-(2S;3R)-3-(2-clorofenil)-2-(2,4-difluorofenil)-oxiranilmetil]-5-tio-cianato-1H-[1,2,4]triazol (B.1.31), 2-[rel-(2S;3R)-3-(2-clorofenil)-2-(2,4-difluorofenil)-oxiranilmetil]-2H-[1,2,4]triazol-3-tiol (B.1.32), 2-[2-cloro-4-(4-clorofenoxi)fenil]-1-(1,2,4-triazol-1-il)pentan-2-ol (B.1.33), 1-[4-(4-clorofenoxi)-2-(trifluorometil)fenil]-1-ciclopropil-2-(1,2,4-triazol-1-il)etanol (B.1.34), 2-[4-(4-clorofenoxi)-2-(trifluorometil)fenil]-1-(1,2,4-triazol-1-il)butan-2-ol (B.1.35), 2-[2-cloro-4-(4-clorofenoxi)fenil]-1-(1,2,4-triazol-1-il)butan-2-ol (B.1.36), ipfentrifluconazol (B.1.37), mefentrifluconazol (B.1.38), 2-[2-cloro-4-(4-clorofenoxi)fenil]-3-metil-1-(1,2,4-triazol-1-il)butan-2-ol (B.1.39), 2-[4-(4-clorofenoxi)-2-(trifluorometil)fenil]-1-(1,2,4-triazol-1-il)pentan-2-ol (B.1.40), 2-[4-(4-fluorofenoxi)-2-(trifluorometil)-fenil]-1-(1,2,4-triazol-1-il)propan-2-ol (B.1.41), 2-[2-cloro-4-(4-clorofenoxi)fenil]-1-(1,2,4-triazol-1-il)pent-3-in-2-ol (B.1.42), 2-(clorometil)-2-metil-5-(p-tolilmetil)-1-(1,2,4-triazol-1-ilmetil)ciclopentanol (B.1.43); imidazoles: imazalil (B.1.44), pefurazoato (B.1.45), procloraz (B.1.46), triflumizol (B.1.47); pirimidinas, piridinas y piperazinas: fenarimol (B.1.49), pirifenox (B.1.50), triforina (B.1.51), [3-(4-cloro-2-fluoro-fenil)-5-(2,4-difluorofenil)isoxazol-4-il]-(3-piridil)metanol (B.1.52); Inhibidores de D14-reductasa: aldimorf (B.2.1), dodemorf (B.2.2), dodemorf-acetato (B.2.3), fenpropimorf (B.2.4), tridemorf (B.2.5), fenpropidin (B.2.6), piperalin (B.2.7), espiroxamina (B.2.8); Inhibidores de 3-ceto reductasa: fenhexamida (B.3.1); Otros inhibidores de la biosíntesis del esterol: clorfenomizol (B.4.1); C) Inhibidores de la síntesis de ácidos nucleicos: Fungicidas de ácido acilamino o fenilamidas: benalaxil (C.1.1), benalaxil-M (C.1.2), kiralaxil (C.1.3), metalaxil (C.1.4), metalaxil-M (C.1.5), ofurace (C.1.6), oxadixil (C.1.7); Otros inhibidores de la síntesis de ácidos nucleicos: himexazol (C.2.1), octilinona (C.2.2), ácido oxolínico (C.2.3), bupirimato (C.2.4), 5-fluorocitosina (C.2.5), 5-fluoro-2-(p-tolilmetoxi)pirimidin-4-amina (C.2.6), 5-fluoro-2-(4-fluorofenilmetoxi)pirimidin-4-amina (C.2.7), 5-fluoro-2-(4-clorofenilmetoxi)pirimidin-4-amina (C.2.8); D) Inhibidores de la división celular y citoesqueleto: Inhibidores de tubulina: benomilo (D.1.1), carbendazima (D.1.2), fuberidazol (D.1.3), tiabendazol (D.1.4), tiofanato-metilo (D.1.5), 3-cloro-4-(2,6-difluorofenil)-6-metil-5-fenil-piridazina (D.1.6), 3-cloro-6-metil-5-fenil-4-(2,4,6-trifluorofenil)piridazina (D.1.7), N-etil-2-[(3-etinil-8-metil-6-quinolil)oxi]butanamida (D.1.8), N-etil-2-[(3-etinil-8-metil-6-quinolil)oxi]-2-metilsulfanil-acetamida (D.1.9), 2-[(3-etinil-8-metil-6-quinolil)oxi]-N-(2-fluoroetil)butanamida (D.1.10), 2-[(3-etinil-8-metil-6-quinolil)oxi]-N-(2-fluoroetil)-2-metoxi-acetamida (D.1.11), 2-[(3-etinil-8-metil-6-quinolil)oxi]-N-propil-butanamida (D.1.12), 2-[(3-etinil-8-metil-6-quinolil)oxi]-2-metoxi-N-propil-acetamida (D.1.13), 2-[(3-etinil-8-metil-6-quinolil)oxi]-2-metilsulfanil-N-propil-acetamida (D.1.14), 2-[(3-etinil-8-metil-6-quinolil)oxi]-N-(2-fluoroetil)-2-metilsulfanil-acetamida (D.1.15), 4-(2-bromo-4-fluoro-fenil)-N-(2-cloro-6-fluoro-fenil)-2,5-dimetil-pirazol-3-amina (D.1.16); Otros inhibidores de la división celular: dietofencarb (D.2.1), etaboxam (D.2.2), pencicurón (D.2.3), fluopicolida (D.2.4), zoxamida (D.2.5), metrafenona (D.2.6), piriofenona (D.2.7); E) Inhibidores de la síntesis de aminoácidos y proteínas: Inhibidores de la síntesis de metionina: ciprodinil (E.1.1), mepanipirim (E.1.2), pirimetanil (E.1.3); Inhibidores de la síntesis de proteínas: blasticidin-S (E.2.1), kasugamicina (E.2.2), kasugamicina clorhidrato-hidrato (E.2.3), mildiomicina (E.2.4), estreptomicina (E.2.5), oxitetraciclina (E.2.6); F) Inhibidores de la transducción de señal: Inhibidores de MAP / histidina quinasa: fluoroimid (F.1.1), iprodiona (F.1.2), procimidona (F.1.3), vinclozolina (F.1.4), fludioxonil (F.1.5); Inhibidores de la proteína G: quinoxifen (F.2.1); G) Inhibidores de la síntesis de lípidos y membrana: Inhibidores de la biosíntesis de fosfolípidos: edifenfós (G.1.1), iprobenfós (G.1.2), pirazofós (G.1.3), isoprotiolano (G.1.4); Peroxidación de lípidos: diclorán (G.2.1), quintoceno (G.2.2), tecnaceno (G.2.3), tolclofós-metilo (G.2.4), bifenilo (G.2.5), cloroneb (G.2.6), etridiazol (G.2.7); Biosíntesis de fosfolípidos y depósito de la pared celular: dimetomorf (G.3.1), flumorf (G.3.2),) mandipropamid (G.3.3), pirimorf (G.3.4), bentiavalicarb (G.3.5), iprovalicarb (G.3.6), valifenalato (G.3.7); Compuestos que afectan la permeabilidad de la membrana celular y ácidos grasos: propamocarb (G.4.1); Inhibidores de la proteína de fijación a oxisterol: oxatiapiprolin (G.5.1), metansulfonato de 2-{3-[2-(1-{[3,5-bis(difluorometil-1H-pirazol-1-il]acetil}piperidin-4-il)-1,3-tiazol-4-il]-4,5-dihidro-1,2-oxazol-5-il}fenilo (G.5.2), metansulfonato de 2-{3-[2-(1-{[3,5-bis(difluorometil)-1H-pirazol-1-il]acetil}piperidin-4-il)-1,3-tiazol-4-il]-4,5-dihidro-1,2-oxazol-5-il}-3-clorofenilo (G.5.3), 4-[1-[2-[3-(difluorometil)-5-metil-pirazol-1-il]acetil]-4-piperidil]-N-tetralin-1-il-piridin-2-carboxamida (G.5.4), 4-[1-[2-[3,5-bis(difluorometil)pirazol-1-il]acetil]-4-piperidil]-N-tetralin-1-il-piridin-2-carboxamida (G.5.5), 4-[1-[2-[3-(difluorometil)-5-(trifluorometil)pirazol-1-il]acetil]-4-piperidil]-N-tetralin-1-il-piridin-2-carboxamida (G.5.6), 4-[1-[2-[5-ciclopropil-3-(difluorometil)pirazol-1-il]acetil]-4-piperidil]-N-tetralin-1-il-piridin-2-carboxamida (G.5.7), 4-[1-[2-[5-metil-3-(trifluorometil)pirazol-1-il]acetil]-4-piperidil]-N-tetralin-1-il-piridin-2-carboxamida (G.5.8), 4-[1-[2-[5-(difluorometil)-3-(trifluorometil)pirazol-1-il]acetil]-4-piperidil]-N-tetralin-1-il-piridin-2-carboxamida (G.5.9), 4-[1-[2-[3,5-bis(trifluorometil)pirazol-1-il]acetil]-4-piperidil]-N-tetralin-1-il-piridin-2-carboxamida (G.5.10), (4-[1-[2-[5-ciclopropil-3-(trifluorometil)pirazol-1-il]acetil]-4-piperidil]-N-tetralin-1-il-piridin-2-carboxamida (G.5.11); H) Inhibidores con acción en múltiples sitios: Sustancias activas inorgánicas: caldo bordelés (H.1.1), cobre (H.1.2), acetato de cobre (H.1.3), hidróxido de cobre (H.1.4), oxicloruro de cobre (H.1.5), sulfato de cobre básico (H.1.6), azufre (H.1.7); Tio- y ditiocarbamatos: ferbam (H.2.1), mancozeb (H.2.2), maneb (H.2.3), metam (H.2.4), metiram (H.2.5), propineb (H.2.6), tiram (H.2.7), zineb (H.2.8), ziram (H.2.9); Compuestos de organocloro: anilazina (H.3.1), clorotalonil (H.3.2), captafol (H.3.3), captán (H.3.4), folpet (H.3.5), diclofluanid (H.3.6), diclorofeno (H.3.7), hexaclorobenceno (H.3.8), pentaclorfenol (H.3.9) y sus sales, ftalida (H.3.10), tolilfluanid (H.3.11); Guanidinas y otros: guanidina (H.4.1), dodina (H.4.2), base libre de dodina (H.4.3), guazatina (H.4.4), guazatina-acetato (H.4.5), iminoctadina (H.4.6), iminoctadina-triacetato (H.4.7), iminoctadina-tris(albesilato) (H.4.8), ditianona (H.4.9), 2,6-dimetil-1H,5H-[1,4]ditiino[2,3-c:5,6-c’]dipirrol-1,3,5,7(2H,6H)-tetraona (H.4.10); I) Inhibidores de la síntesis de la pared celular: Inhibidores de la síntesis de glucano: validamicina (I.1.1), polioxina B (I.1.2); Inhibidores de la síntesis de melanina: piroquilona (I.2.1), triciclazol (I.2.2), carpropamida (I.2.3), diciclomet (I.2.4), fenoxanil (I.2.5); J) Inductores de la defensa de la planta: Acibenzolar-S-metilo (J.1.1), probenazol (J.1.2), isotianil (J.1.3), tiadinil (J.1.4), prohexadiona-calcio (J.1.5); fosfonatos: fosetil (J.1.6), fosetil-aluminio (J.1.7), ácido fosforoso y sus sales (J.1.8), bicarbonato de potasio o sodio (J.1.9), 4-ciclopropil-N-(2,4-dimetoxifenil)tiadiazol-5-carboxamida (J.1.10), fosfonato de calcio (J.1.11), fosfonato de potasio (J.1.12); K) Modo de acción desconocido: Bronopol (K.1.1), quinometionato (K.1.2), ciflufenamida (K.1.3), cimoxanilo (K.1.4), dazomet (K.1.5), debacarb (K.1.6), diclocimet (K.1.7), diclomezina (K.1.8), difenzoquat (K.1.9), difenzoquat-metilsulfato (K.1.10), difenilamina (K.1.11), fenitropan (K.1.12), fenpirazamina (K.1.13), flumetover (K.1.14), flusulfamida (K.1.15), flutianil (K.1.16), harpin (K.1.17), metasulfocarb (K.1.18), nitrapirin (K.1.19), nitrotal-isopropilo (K.1.20), tolprocarb (K.1.21), oxina-cobre (K.1.22), proquinazid (K.1.23), tebufloquina (K.1.24), tecloftalam (K.1.25), triazóxido (K.1.26), N’-(4-(4-cloro-3-trifluorometil-fenoxi)-2,5-dimetil-fenil)-N-etil-N-metilformamidina (K.1.27), N’-(4-(4-fluoro-3-trifluorometil-fenoxi)-2,5-dimetil-fenil)-N-etil-N-metilformamidina (K.1.28), N’-[4-[[3-[(4-clorofenil)metil]-1,2,4-tiadiazol-5-il]oxi]-2,5-dimetil-fenil]-N-etil-N-metil-formamidina (K.1.29), N’-(5-bromo-6-indan-2-iloxi-2-metil-3-piridil)-N-etil-N-metil-formamidina (K.1.30), N’-[5-bromo-6-[1-(3,5-difluorofenil)etoxi]-2-metil-3-piridil]-N-etil-N-metil-formamidina (K.1.31), N’-[5-bromo-6-(4-isopropilciclohexoxi)-2-metil-3-piridil]-N-etil-N-metil-formamidina (K.1.32), N’-[5-bromo-2-metil-6-(1-feniletoxi)-3-piridil]-N-etil-N-metil-formamidina (K.1.33), N’-(2-metil-5-trifluorometil-4-(3-trimetil-silanil-propoxi)-fenil)-N-etil-N-metilformamidina (K.1.34), N’-(5-difluorometil-2-metil-4-(3-trimetilsilanil-propoxi)-fenil)-N-etil-N-metilformamidina (K.1.35), 2-(4-cloro-fenil)-N-[4-(3,4-dimetoxi-fenil)-isoxazol-5-il]-2-prop-2-iniloxi-acetamida (K.1.36), 3-[5-(4-cloro-fenil)-2,3-dimetil-isoxazolidin-3-il]-piridina (prisoxazol) (K.1.37), 3-[5-(4-metilfenil)-2,3-dimetil-isoxazolidin-3-il]-piridina (K.1.38), 5-cloro-1-(4,6-dimetoxi-pirimidin-2-il)-2-metil-1H-benzoimidazol (K.1.39), (Z)-3-amino-2-ciano-3-fenil-prop-2-enoato de etilo (K.1.40), picarbutrazox (K.1.41), N-[6-[[(Z)-[(1-metiltetrazol-5-il)-fenil-metilen]amino]oximetil]-2-piridil]carbamato de pentilo (K.1.42), but-3-inil N-[6-[[(Z)-[(1-metiltetrazol-5-il)-fenil-metilen]amino]oximetil]-2-piridil]carbamato (K.1.43), 2-[2-[(7,8-difluoro-2-metil-3-quinolil)oxi]-6-fluoro-fenil]propan-2-ol (K.1.44), 2-[2-fluoro-6-[(8-fluoro-2-metil-3-quinolil)oxi]fenil]propan-2-ol (K.1.45), 3-(5-fluoro-3,3,4,4-tetrametil-3,4-dihidroisoquinolin-1-il)quinolina (K.1.46), quinofumelin (K.1.47), 3-(4,4,5-trifluoro-3,3-dimetil-3,4-dihidroisoquinolin-1-il)quinolina (K.1.48), 9-fluoro-2,2-dimetil-5-(3-quinolil)-3H-1,4-benzoxazepina (K.1.49), 2-(6-bencil-2-piridil)quinazolina (K.1.50), 2-[6-(3-fluoro-4-metoxi-fenil)-5-metil-2-piridil]quinazolina (K.1.51), diclobentiazox (K.1.52), N’-(2,5-dimetil-4-fenoxi-fenil)-N-etil-N-metil-formamidina (K.1.53), N’-[5-bromo-2-metil-6-(1-metil-2-propoxi-etoxi)-3-piridil]-N-etil-N-metil-formamidina (K.1.54); M) Reguladores del crecimiento: ácido abscísico (M.1.1), amidoclor, ancimidol, 6-bencilaminopurina, brasinolida, butralina, clormequat, cloruro de clormequat, cloruro de colina, ciclanilida, daminozida, diquegulac, dimetipina, 2,6-dimetilpuridina, etefón, flumetralina, flurprimidol, flutiacet, forclorfenurón, ácido giberélico, inabenfida, ácido indol-3-acético, hidrazida maleica, mefluidida, mepiquat, cloruro de mepiquat, ácido naftalenacético, N-6-benciladenina, paclobutrazol, prohexadiona, prohexadiona-calcio, prohidrojasmona, tidiazurona, triapentenol, fosforotritioato de tributilo, ácido 2,3,5-tri-iodobenzoico, trinexapac-etilo y uniconazol; N) Herbicidas de las clases N.1 a N.15: N.1) Inhibidores de la biosíntesis de lípidos: aloxidim (N.1.1), aloxidim-sodio (N.1.2), butroxidim (N.1.3), cletodim (N.1.4), clodinafop (N.1.5), clodinafop-propargilo (N.1.6), cicloxidim (N.1.7), cihalofop (N.1.8), cihalofop-butilo (N.1.9), diclofop (N.1.10), diclofop-metilo (N.1.11), fenoxaprop (N.1.12), fenoxaprop-etilo (N.1.13), fenoxaprop-P (N.1.14), fenoxaprop-P-etilo (N.1.15), fluazifop (N.1.16), fluazifop-butilo (N.1.17), fluazifop-P (N.1.18), fluazifop-P-butilo (N.1.19), haloxifop (N.1.20), haloxifop-metilo (N.1.21), haloxifop-P (N.1.22), haloxifop-P-metilo (N.1.23), metamifop (N.1.24), pinoxaden (N.1.25), profoxidim (N.1.26), propaquizafop (N.1.27), quizalofop (N.1.28), quizalofop-etilo (N.1.29), quizalofop-tefurilo (N.1.30), quizalofop-P (N.1.31), quizalofop-P-etilo (N.1.32), quizalofop-P-tefurilo (N.1.33), setoxidim (N.1.34), tepraloxidim (N.1.35), tralcoxidim (N.1.36), 4-(4’-cloro-4-ciclopropil-2’-fluoro[1,1’-bifenil]-3-il)-5-hidroxi-2,2,6,6-tetrametil-2H-piran-3(6H)-ona ((N.1.37) CAS 1312337-72-6); 4-(2’,4’-dicloro-4-ciclopropil[1,1’-bifenil]-3-il)-5-hidroxi-2,2,6,6-tetrametil-2H-piran-3(6H)-ona ((N.1.38) CAS 1312337-45-3); 4-(4’-cloro-4-etil-2’-fluoro[1,1’-bifenil]-3-il)-5-hidroxi-2,2,6,6-tetrametil-2H-piran-3(6H)-ona ((N.1.39) CAS 1033757-93-5); 4-(2’,4’-dicloro-4-etil[1,1’-bifenil]-3-il)-2,2,6,6-tetrametil-2H-piran-3,5(4H,6H)-diona ((N.1.40) CAS 1312340-84-3); 5-(acetiloxi)-4-(4’-cloro-4-ciclopropil-2’-fluoro[1,1’-bifenil]-3-il)-3,6-dihidro-2,2,6,6-tetrametil-2H-piran-3-ona ((N.1.41) CAS 1312337-48-6); 5-(acetiloxi)-4-(2’,4’-dicloro-4-ciclopropil-[1,1’-bifenil]-3-il)-3,6-dihidro-2,2,6,6-tetrametil-2H-piran-3-ona (N.1.42); 5-(acetiloxi)-4-(4’-cloro-4-etil-2’-fluoro[1,1’-bifenil]-3-il)-3,6-dihidro-2,2,6,6-tetrametil-2H-piran-3-ona ((N.1.43) CAS 1312340-82-1); 5-(acetiloxi)-4-(2’,4’-dicloro-4-etil[1,1’-bifenil]-3-il)-3,6-dihidro-2,2,6,6-tetrametil-2H-piran-3-ona ((N.1.44) CAS 1033760-55-2); metiléster del ácido 4-(4’-cloro-4-ciclopropil-2’-fluoro[1,1’-bifenil]-3-il)-5,6-dihidro-2,2,6,6-tetrametil-5-oxo-2H-piran-3-il carbónico ((N.1.45) CAS 1312337-51-1); metiléster del ácido 4-(2’,4’-dicloro-4-ciclopropil-[1,1’-bifenil]-3-il)-5,6-dihidro-2,2,6,6-tetrametil-5-oxo-2H-piran-3-il carbónico (N.1.46); metiléster del ácido 4-(4’-cloro-4-etil-2’-fluoro[1,1’-bifenil]-3-il)-5,6-dihidro-2,2,6,6-tetrametil-5-oxo-2H-piran-3-il carbónico ((N.1.47) CAS 1312340-83-2); metiléster del ácido 4-(2’,4’-dicloro-4-etil[1,1’-bifenil]-3-il)-5,6-dihidro-2,2,6,6-tetrametil-5-oxo-2H-piran-3-il carbónico ((N.1.48) CAS 1033760-58-5); benfuresato (N.1.49), butilato (N.1.50), cicloato (N.1.51), dalapón (N.1.52), dimepiperato (N.1.53), EPTC (N.1.54), esprocarb (N.1.55), etofumesato (N.1.56), flupropanato (N.1.57), molinato (N.1.58), orbencarb (N.1.59), pebulato (N.1.60), prosulfocarb (N.1.61), TCA (N.1.62), tiobencarb (N.1.63), tiocarbazilo (N.1.64), trialato (N.1.65) y vernolato (N.1.66); N.2) Inhibidores de ALS: amidosulfurón (N.2.1), azimsulfurón (N.2.2), bensulfurón (N.2.3), bensulfurón-metilo (N.2.4), clorimurón (N.2.5), clorimurón-etilo (N.2.6), clorsulfurón (N.2.7), cinosulfurón (N.2.8), ciclosulfamurón (N.2.9), etametsulfurón (N.2.10), etametsulfurón-metilo (N.2.11), etoxisulfurón (N.2.12), flazasulfurón (N.2.13), flucetosulfurón (N.2.14), flupirsulfurón (N.2.15), flupirsulfurón-metil-sodio (N.2.16), foramsulfurón (N.2.17), halosulfurón (N.2.18), halosulfurón-metilo (N.2.19), imazosulfurón (N.2.20), iodosulfurón (N.2.21), iodosulfurón-metil-sodio (N.2.22), iofensulfurón (N.2.23), iofensulfurón-sodio (N.2.24), mesosulfurón (N.2.25), metazosulfurón (N.2.26), metsulfurón (N.2.27), metsulfurón-metilo (N.2.28), nicosulfurón (N.2.29), ortosulfamurón (N.2.30), oxasulfurón (N.2.31), primisulfurón (N.2.32), primisulfurón-metilo (N.2.33), propirisulfurón (N.2.34), prosulfurón (N.2.35), pirazosulfurón (N.2.36), pirazosulfurón-etilo (N.2.37), rimsulfurón (N.2.38), sulfometurón (N.2.39), sulfometurón-metilo (N.2.40), sulfosulfurón (N.2.41), tifensulfurón (N.2.42), tifensulfurón-metilo (N.2.43), triasulfurón (N.2.44), tribenurón (N.2.45), tribenurón-metilo (N.2.46), trifloxisulfurón (N.2.47), triflusulfurón (N.2.48), triflusulfurón-metilo (N.2.49), tritosulfurón (N.2.50), imazametabenz (N.2.51), imazametabenz-metilo (N.2.52), imazamox (N.2.53), imazapic (N.2.54), imazapir (N.2.55), imazaquin (N.2.56), imazetapir (N.2.57); cloransulam (N.2.58), cloransulam-metilo (N.2.59), diclosulam (N.2.60), flumetsulam (N.2.61), florasulam (N.2.62), metosulam (N.2.63), penoxsulam (N.2.64), pirimisulfán (N.2.65) y piroxsulam (N.2.66); bispiribac (N.2.67), bispiribac-sodio (N.2.68), piribenzoxim (N.2.69), piriftalid (N.2.70), piriminobac (N.2.71), piriminobac-metilo (N.2.72), piritiobac (N.2.73), piritiobac-sodio (N.2.74), 1-metiletiléster del ácido 4-[[[2-[(4,6-dimetoxi-2-pirimidinil)oxi]fenil]metil]amino]-benzoico ((N.2.75) CAS 420138-41-6), propiléster del ácido 4-[[[2-[(4,6-dimetoxi-2-pirimidinil)oxi]fenil]metil]amino]-benzoico ((N.2.76) CAS 420138-40-5), N-(4-bromofenil)-2-[(4,6-dimetoxi-2-pirimidinil)oxi]bencenmetanamina ((N.2.77) CAS 420138-01-8); flucarbazona (N.2.78), flucarbazona-sodio (N.2.79), propoxicarbazona (N.2.80), propoxicarbazona-sodio (N.2.81), tiencarbazona (N.2.82), tiencarbazona-metilo (N.2.83), triafamona (N.2.84); N.3) Inhibidores de la fotosíntesis: amicarbazona (N.3.1); clorotriazina (N.3.2); ametrina (N.3.3), atrazina (N.3.4), cloridazona (N.3.5), cianazina (N.3.6), desmetrina (N.3.7), dimetametrina (N.3.8), hexazinona (N.3.9), metribuzina (N.3.10), prometón (N.3.11), prometrina (N.3.12), propazina (N.3.13), simazina (N.3.14), simetrina (N.3.15), terbumetón (N.3.16), terbutilazina (N.3.17), terbutrina (N.3.18), trietazina (N.3.19); clorobromurón (N.3.20), clorotolurón (N.3.21), cloroxurón (N.3.22), dimefurón (N.3.23), diurón (N.3.24), fluometurón (N.3.25), isoproturón (N.3.26), isourón (N.3.27), linurón (N.3.28), metamitrón (N.3.29), metabenztiazurón (N.3.30), metobenzurón (N.3.31), metoxurón (N.3.32), monolinurón (N.3.33), neburón (N.3.34), sidurón (N.3.35), tebutiurón (N.3.36), tiadiazurón (N.3.37), desmedifam (N.3.38), karbutilat (N.3.39), fenmedifam (N.3.40), fenmedifam-etilo (N.3.41), bromofenoxim (N.3.42), bromoxinil (N.3.43) y sus sales y ésteres, ioxinil (N.3.44) y sus sales y ésteres, bromacil (N.3.45), lenacil (N.3.46), terbacil (N.3.47), bentazón (N.3.48), bentazón-sodio (N.3.49), piridato (N.3.50), piridafol (N.3.51), pentanoclor (N.3.52), propanilo (N.3.53); diquat (N.3.54), diquat-dibromuro (N.3.55), paraquat (N.3.56), paraquat-dicloruro (N.3.57), paraquat-dimetilsulfato (N.3.58); N.4) Inhibidores de la protoporfirinógeno-IX oxidasa: acifluorfen (N.4.1), acifluorfen-sodio (N.4.2), azafenidina (N.4.3), bencarbazona (N.4.4), benzfendizona (N.4.5), bifehox (N.4.6), butafenacil (N.4.7), carfentrazona (N.4.8), carfentrazona-etilo (N.4.9), clormetoxifen (N.4.10), cinidon-etilo (N.4.11), fluazolato (N.4.12), flufenpir (N.4.13), flufenpir-etilo (N.4.14), flumiclorac (N.4.15), flumiclorac-pentilo (N.4.16), flumioxazina (N.4.17), fluoroglicofen (N.4.18), fluoroglicofen-etilo (N.4.19), flutiacet (N.4.20), flutiacet-metilo (N.4.21), fomesafen (N.4.22), halosafen (N.4.23), lactofen (N.4.24), oxadiargilo (N.4.25), oxadiazón (N.4.26), oxifluorfen (N.4.27), pentoxazona (N.4.28), profluazol (N.4.29), piraclonil (N.4.30), piraflufen (N.4.31), piraflufen-etilo (N.4.32), saflufenacil (N.4.33), sulfentrazona (N.4.34), tidiazimin (N.4.35), tiafenacil (N.4.36), trifludimoxazin (N.4.37), etil [3-[2-cloro-4-fluoro-5-(1-metil-6-trifluorometil-2,4-dioxo-1,2,3,4-tetrahidropirimidin-3-il)fenoxi]-2-piridiloxi]acetato ((N.4.38) CAS 353292-31-6), N-etil-3-(2,6-dicloro-4-trifluoro-metilfenoxi)-5-metil-1H-pirazol-1-carboxamida ((N.4.39) CAS 4520988-92-9), N-tetrahidrofurfuril-3-(2,6-dicloro-4-trifluorometilfenoxi)-5-metil-1H-pirazol-1-carboxamida ((N.4.40) CAS 915396-43-9), N-etil-3-(2-cloro-6-fluoro-4-trifluorometilfenoxi)-5-metil-1H-pirazol-1-carboxamida ((N.4.41) CAS 452099-05-7), N-tetrahidrofurfuril-3-(2-cloro-6-fluoro-4-trifluorometilfenoxi)-5-metil-1H-pirazol-1-carboxamida ((N.4.42) CAS 452100-03-7), 3-[7-fluoro-3-oxo-4-(prop-2-inil)-3,4-dihidro-2H-benzo[1,4]oxazin-6-il]-1,5-dimetil-6-tioxo-[1,3,5]triazinan-2,4-diona ((N.4.43) CAS 451484-50-7), 2-(2,2,7-trifluoro-3-oxo-4-prop-2-inil-3,4-dihidro-2H-benzo[1,4]oxazin-6-il)-4,5,6,7-tetrahidro-isoindol-1,3-diona ((N.4.44) CAS 1300118-96-0), 1-metil-6-trifluorometil-3-(2,2,7-trifluoro-3-oxo-4-prop-2-inil-3,4-dihidro-2H-benzo[1,4]oxazin-6-il)-1H-pirimidin-2,4-diona ((N.4.45) CAS 1304113-05-0), metil (E)-4-[2-cloro-5-[4-cloro-5-(difluorometoxi)-1H-metil-pirazol-3-il]-4-fluoro-fenoxi]-3-metoxi-but-2-enoato ((N.4.46) CAS 948893-00-3), 3-[7-cloro-5-fluoro-2-(trifluorometil)-1H-bencimidazol-4-il]-1-metil-6-(tr
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| JP6107377B2 (ja) | 2012-04-27 | 2017-04-05 | 住友化学株式会社 | テトラゾリノン化合物及びその用途 |
| CN103387541B (zh) | 2012-05-10 | 2016-02-10 | 中国中化股份有限公司 | 一种取代吡唑醚类化合物的制备方法 |
| WO2014060177A1 (en) | 2012-10-16 | 2014-04-24 | Syngenta Participations Ag | Fungicidal compositions |
| WO2015065922A1 (en) | 2013-10-28 | 2015-05-07 | Dexcom, Inc. | Devices used in connection with continuous analyte monitoring that provide the user with one or more notifications, and related methods |
| EP2865265A1 (en) | 2014-02-13 | 2015-04-29 | Bayer CropScience AG | Active compound combinations comprising phenylamidine compounds and biological control agents |
| EP3151669B1 (en) | 2014-06-06 | 2020-10-28 | Basf Se | Use of substituted oxadiazoles for combating phytopathogenic fungi |
| CA3002299A1 (en) | 2015-11-05 | 2017-05-11 | Basf Se | Substituted oxadiazoles for combating phytopathogenic fungi |
| AR106679A1 (es) | 2015-11-13 | 2018-02-07 | Basf Se | Oxadiazoles sustituidos para combatir hongos fitopatógenos |
| JP2018537457A (ja) | 2015-11-19 | 2018-12-20 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 植物病原菌を駆除するための置換オキサジアゾール |
| CR20180332A (es) * | 2015-11-19 | 2018-10-18 | Basf Se | Oxadiazoles sustituidos para combatir hongos fitopatógenos |
| JP2019500337A (ja) | 2015-12-03 | 2019-01-10 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 植物病原菌を駆除するための置換オキサジアゾール |
| CN108884062A (zh) | 2016-04-11 | 2018-11-23 | 巴斯夫欧洲公司 | 用于防治植物病原性真菌的取代噁二唑类 |
| AR108745A1 (es) * | 2016-06-21 | 2018-09-19 | Syngenta Participations Ag | Derivados de oxadiazol microbiocidas |
-
2018
- 2018-04-19 EP EP18718463.5A patent/EP3618629A1/en not_active Withdrawn
- 2018-04-19 WO PCT/EP2018/059984 patent/WO2018202428A1/en not_active Ceased
- 2018-04-19 EA EA201992550A patent/EA201992550A1/ru unknown
- 2018-04-19 US US16/610,182 patent/US20210084902A1/en not_active Abandoned
- 2018-04-27 AR ARP180101112A patent/AR111629A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR112019023117A2 (pt) | 2020-05-26 |
| US20210084902A1 (en) | 2021-03-25 |
| WO2018202428A1 (en) | 2018-11-08 |
| EA201992550A1 (ru) | 2020-04-14 |
| EP3618629A1 (en) | 2020-03-11 |
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