AR071332A1 - Composiciones fungicidas - Google Patents
Composiciones fungicidasInfo
- Publication number
- AR071332A1 AR071332A1 ARP090100125A ARP090100125A AR071332A1 AR 071332 A1 AR071332 A1 AR 071332A1 AR P090100125 A ARP090100125 A AR P090100125A AR P090100125 A ARP090100125 A AR P090100125A AR 071332 A1 AR071332 A1 AR 071332A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- compound
- formula
- dodianimone
- difluoromethyl
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title abstract 11
- 239000000417 fungicide Substances 0.000 title abstract 10
- 239000000203 mixture Substances 0.000 title abstract 4
- -1 2-chloro-6-fluoro-phenyl Chemical group 0.000 abstract 25
- 150000001875 compounds Chemical class 0.000 abstract 14
- AQFWNELGMODZGC-UHFFFAOYSA-N o-ethylhydroxylamine Chemical compound CCON AQFWNELGMODZGC-UHFFFAOYSA-N 0.000 abstract 8
- 125000001544 thienyl group Chemical group 0.000 abstract 3
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 2
- 239000005802 Mancozeb Substances 0.000 abstract 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract 2
- 229930182692 Strobilurin Natural products 0.000 abstract 2
- 239000005941 Thiamethoxam Substances 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
- YKYOUMDCQGMQQO-UHFFFAOYSA-L cadmium dichloride Chemical compound Cl[Cd]Cl YKYOUMDCQGMQQO-UHFFFAOYSA-L 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-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
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- DBTLWVMHSCKUSJ-UHFFFAOYSA-N dithian-3-amine Chemical compound NC1CCCSS1 DBTLWVMHSCKUSJ-UHFFFAOYSA-N 0.000 abstract 2
- 239000002917 insecticide Substances 0.000 abstract 2
- 239000000463 material Substances 0.000 abstract 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 abstract 2
- 244000045561 useful plants Species 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
- OZFAFGSSMRRTDW-UHFFFAOYSA-N (2,4-dichlorophenyl) benzenesulfonate Chemical compound ClC1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=CC=C1 OZFAFGSSMRRTDW-UHFFFAOYSA-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
- SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-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
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 abstract 1
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-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
- 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
- CPZLRDXKLHKMQX-UHFFFAOYSA-N 1,1-bis(4-chlorophenyl)-2-ethoxyethanol Chemical compound C=1C=C(Cl)C=CC=1C(O)(COCC)C1=CC=C(Cl)C=C1 CPZLRDXKLHKMQX-UHFFFAOYSA-N 0.000 abstract 1
- ZAIDIVBQUMFXEC-UHFFFAOYSA-N 1,1-dichloroprop-1-ene Chemical compound CC=C(Cl)Cl ZAIDIVBQUMFXEC-UHFFFAOYSA-N 0.000 abstract 1
- TUBQDCKAWGHZPF-UHFFFAOYSA-N 1,3-benzothiazol-2-ylsulfanylmethyl thiocyanate Chemical compound C1=CC=C2SC(SCSC#N)=NC2=C1 TUBQDCKAWGHZPF-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
- SVPKNMBRVBMTLB-UHFFFAOYSA-N 2,3-dichloronaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(Cl)=C(Cl)C(=O)C2=C1 SVPKNMBRVBMTLB-UHFFFAOYSA-N 0.000 abstract 1
- OWDLFBLNMPCXSD-UHFFFAOYSA-N 2-chloro-N-(2,6-dimethylphenyl)-N-(2-oxotetrahydrofuran-3-yl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)C1C(=O)OCC1 OWDLFBLNMPCXSD-UHFFFAOYSA-N 0.000 abstract 1
- ADRPZEYTIFWCBC-UHFFFAOYSA-N 2-fluoro-n-methyl-n-naphthalen-1-ylacetamide Chemical compound C1=CC=C2C(N(C(=O)CF)C)=CC=CC2=C1 ADRPZEYTIFWCBC-UHFFFAOYSA-N 0.000 abstract 1
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 abstract 1
- FSCWZHGZWWDELK-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-5-ethenyl-5-methyl-2,4-oxazolidinedione Chemical compound O=C1C(C)(C=C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FSCWZHGZWWDELK-UHFFFAOYSA-N 0.000 abstract 1
- XHTZYMTVLCHVLD-UHFFFAOYSA-N 3-(difluoromethyl)-1-methyl-n-[2-(1,1,2,2-tetrafluoroethoxy)phenyl]pyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1OC(F)(F)C(F)F XHTZYMTVLCHVLD-UHFFFAOYSA-N 0.000 abstract 1
- RLOHOBNEYHBZID-UHFFFAOYSA-N 3-(difluoromethyl)-1-methylpyrazole-4-carboxylic acid Chemical compound CN1C=C(C(O)=O)C(C(F)F)=N1 RLOHOBNEYHBZID-UHFFFAOYSA-N 0.000 abstract 1
- WYVVKGNFXHOCQV-UHFFFAOYSA-N 3-iodoprop-2-yn-1-yl butylcarbamate Chemical compound CCCCNC(=O)OCC#CI WYVVKGNFXHOCQV-UHFFFAOYSA-N 0.000 abstract 1
- NEKULYKCZPJMMJ-UHFFFAOYSA-N 5-chloro-N-{1-[4-(difluoromethoxy)phenyl]propyl}-6-methylpyrimidin-4-amine Chemical compound C=1C=C(OC(F)F)C=CC=1C(CC)NC1=NC=NC(C)=C1Cl NEKULYKCZPJMMJ-UHFFFAOYSA-N 0.000 abstract 1
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 abstract 1
- 239000005660 Abamectin Substances 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- 239000005964 Acibenzolar-S-methyl Substances 0.000 abstract 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 abstract 1
- DJHGAFSJWGLOIV-UHFFFAOYSA-K Arsenate3- Chemical class [O-][As]([O-])([O-])=O DJHGAFSJWGLOIV-UHFFFAOYSA-K 0.000 abstract 1
- 239000005730 Azoxystrobin Substances 0.000 abstract 1
- 239000005734 Benalaxyl Substances 0.000 abstract 1
- 239000005735 Benalaxyl-M Substances 0.000 abstract 1
- 239000005736 Benthiavalicarb Substances 0.000 abstract 1
- 239000005739 Bordeaux mixture Substances 0.000 abstract 1
- 239000005740 Boscalid Substances 0.000 abstract 1
- 239000005742 Bupirimate Substances 0.000 abstract 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 abstract 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
- 239000005747 Chlorothalonil Substances 0.000 abstract 1
- 239000005498 Clodinafop Substances 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 abstract 1
- 239000005750 Copper hydroxide Substances 0.000 abstract 1
- 239000005756 Cymoxanil Substances 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 abstract 1
- 239000005767 Epoxiconazole Substances 0.000 abstract 1
- 239000005976 Ethephon Substances 0.000 abstract 1
- FANWXYMNYCJKBC-UHFFFAOYSA-N FCC1(NN(C=C1C(=O)O)C)CF Chemical compound FCC1(NN(C=C1C(=O)O)C)CF FANWXYMNYCJKBC-UHFFFAOYSA-N 0.000 abstract 1
- 239000005774 Fenamidone Substances 0.000 abstract 1
- IWDQPCIQCXRBQP-UHFFFAOYSA-M Fenaminosulf Chemical compound [Na+].CN(C)C1=CC=C(N=NS([O-])(=O)=O)C=C1 IWDQPCIQCXRBQP-UHFFFAOYSA-M 0.000 abstract 1
- 239000005958 Fenamiphos (aka phenamiphos) Substances 0.000 abstract 1
- 239000005776 Fenhexamid Substances 0.000 abstract 1
- 239000005780 Fluazinam Substances 0.000 abstract 1
- 239000005789 Folpet Substances 0.000 abstract 1
- 239000005791 Fuberidazole Substances 0.000 abstract 1
- 239000005562 Glyphosate Substances 0.000 abstract 1
- 239000005906 Imidacloprid Substances 0.000 abstract 1
- 239000005797 Iprovalicarb Substances 0.000 abstract 1
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 abstract 1
- YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical compound [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 abstract 1
- KYGZCKSPAKDVKC-UHFFFAOYSA-N Oxolinic acid Chemical compound C1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC2=C1OCO2 KYGZCKSPAKDVKC-UHFFFAOYSA-N 0.000 abstract 1
- 239000004100 Oxytetracycline Substances 0.000 abstract 1
- 239000005985 Paclobutrazol Substances 0.000 abstract 1
- 239000005662 Paraffin oil Substances 0.000 abstract 1
- 229930040373 Paraformaldehyde Natural products 0.000 abstract 1
- 239000005597 Pinoxaden Substances 0.000 abstract 1
- 239000005821 Propamocarb Substances 0.000 abstract 1
- 239000005822 Propiconazole Substances 0.000 abstract 1
- 239000005823 Propineb Substances 0.000 abstract 1
- 239000005824 Proquinazid Substances 0.000 abstract 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005842 Thiophanate-methyl Substances 0.000 abstract 1
- 239000005847 Triazoxide Substances 0.000 abstract 1
- 229930195482 Validamycin Natural products 0.000 abstract 1
- 239000005870 Ziram Substances 0.000 abstract 1
- 239000005863 Zoxamide Substances 0.000 abstract 1
- 229950008167 abamectin Drugs 0.000 abstract 1
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical group CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 239000011717 all-trans-retinol Substances 0.000 abstract 1
- 235000019169 all-trans-retinol Nutrition 0.000 abstract 1
- 239000001099 ammonium carbonate Substances 0.000 abstract 1
- 235000012501 ammonium carbonate Nutrition 0.000 abstract 1
- IMHBYKMAHXWHRP-UHFFFAOYSA-N anilazine Chemical compound ClC1=CC=CC=C1NC1=NC(Cl)=NC(Cl)=N1 IMHBYKMAHXWHRP-UHFFFAOYSA-N 0.000 abstract 1
- XQMIGRUKENWSIJ-UHFFFAOYSA-N aniline;pyrimidine Chemical compound C1=CN=CN=C1.NC1=CC=CC=C1 XQMIGRUKENWSIJ-UHFFFAOYSA-N 0.000 abstract 1
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 abstract 1
- CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 abstract 1
- LJOZMWRYMKECFF-UHFFFAOYSA-N benodanil Chemical compound IC1=CC=CC=C1C(=O)NC1=CC=CC=C1 LJOZMWRYMKECFF-UHFFFAOYSA-N 0.000 abstract 1
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 abstract 1
- VVSLYIKSEBPRSN-PELKAZGASA-N benthiavalicarb Chemical compound C1=C(F)C=C2SC([C@@H](C)NC(=O)[C@@H](NC(O)=O)C(C)C)=NC2=C1 VVSLYIKSEBPRSN-PELKAZGASA-N 0.000 abstract 1
- USRKFGIXLGKMKU-ABAIWWIYSA-N benthiavalicarb-isopropyl Chemical compound C1=C(F)C=C2SC([C@@H](C)NC(=O)[C@H](C(C)C)NC(=O)OC(C)C)=NC2=C1 USRKFGIXLGKMKU-ABAIWWIYSA-N 0.000 abstract 1
- SECBZPQAVAPMDC-UHFFFAOYSA-N benzhydrylbenzene hydrate Chemical compound O.C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 SECBZPQAVAPMDC-UHFFFAOYSA-N 0.000 abstract 1
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 abstract 1
- CXNPLSGKWMLZPZ-UHFFFAOYSA-N blasticidin-S Natural products O1C(C(O)=O)C(NC(=O)CC(N)CCN(C)C(N)=N)C=CC1N1C(=O)N=C(N)C=C1 CXNPLSGKWMLZPZ-UHFFFAOYSA-N 0.000 abstract 1
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 abstract 1
- 229940118790 boscalid Drugs 0.000 abstract 1
- DSKJPMWIHSOYEA-UHFFFAOYSA-N bupirimate Chemical compound CCCCC1=C(C)N=C(NCC)N=C1OS(=O)(=O)N(C)C DSKJPMWIHSOYEA-UHFFFAOYSA-N 0.000 abstract 1
- JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 abstract 1
- 239000006013 carbendazim Substances 0.000 abstract 1
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 abstract 1
- QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 abstract 1
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 abstract 1
- RXDMAYSSBPYBFW-UHFFFAOYSA-N carpropamid Chemical compound C=1C=C(Cl)C=CC=1C(C)NC(=O)C1(CC)C(C)C1(Cl)Cl RXDMAYSSBPYBFW-UHFFFAOYSA-N 0.000 abstract 1
- 229940119201 cedar leaf oil Drugs 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- PFIADAMVCJPXSF-UHFFFAOYSA-N chloroneb Chemical compound COC1=CC(Cl)=C(OC)C=C1Cl PFIADAMVCJPXSF-UHFFFAOYSA-N 0.000 abstract 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 abstract 1
- 229940117916 cinnamic aldehyde Drugs 0.000 abstract 1
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 abstract 1
- YUIKUTLBPMDDNQ-MRVPVSSYSA-N clodinafop Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=NC=C(Cl)C=C1F YUIKUTLBPMDDNQ-MRVPVSSYSA-N 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 229910001956 copper hydroxide Inorganic materials 0.000 abstract 1
- 229910000365 copper sulfate Inorganic materials 0.000 abstract 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 abstract 1
- BIXZHMJUSMUDOQ-UHFFFAOYSA-N dichloran Chemical compound NC1=C(Cl)C=C([N+]([O-])=O)C=C1Cl BIXZHMJUSMUDOQ-UHFFFAOYSA-N 0.000 abstract 1
- UWQMKVBQKFHLCE-UHFFFAOYSA-N diclomezine Chemical compound C1=C(Cl)C(C)=C(Cl)C=C1C1=NNC(=O)C=C1 UWQMKVBQKFHLCE-UHFFFAOYSA-N 0.000 abstract 1
- WXGQGFXJEPGZCS-UHFFFAOYSA-J dicopper octanoate Chemical compound C(CCCCCCC)(=O)[O-].[Cu+2].[Cu+2].C(CCCCCCC)(=O)[O-].C(CCCCCCC)(=O)[O-].C(CCCCCCC)(=O)[O-] WXGQGFXJEPGZCS-UHFFFAOYSA-J 0.000 abstract 1
- CJHXCRMKMMBYJQ-UHFFFAOYSA-N dimethirimol Chemical compound CCCCC1=C(C)NC(N(C)C)=NC1=O CJHXCRMKMMBYJQ-UHFFFAOYSA-N 0.000 abstract 1
- OPGYRRGJRBEUFK-UHFFFAOYSA-L disodium;diacetate Chemical compound [Na+].[Na+].CC([O-])=O.CC([O-])=O OPGYRRGJRBEUFK-UHFFFAOYSA-L 0.000 abstract 1
- CXEGAUYXQAKHKJ-NSBHKLITSA-N emamectin B1a Chemical compound C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](NC)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 CXEGAUYXQAKHKJ-NSBHKLITSA-N 0.000 abstract 1
- IGUYEXXAGBDLLX-UHFFFAOYSA-N ethyl 3-(3,5-dichlorophenyl)-5-methyl-2,4-dioxo-1,3-oxazolidine-5-carboxylate Chemical compound O=C1C(C(=O)OCC)(C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 IGUYEXXAGBDLLX-UHFFFAOYSA-N 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- LMVPQMGRYSRMIW-KRWDZBQOSA-N fenamidone Chemical compound O=C([C@@](C)(N=C1SC)C=2C=CC=CC=2)N1NC1=CC=CC=C1 LMVPQMGRYSRMIW-KRWDZBQOSA-N 0.000 abstract 1
- ZCJPOPBZHLUFHF-UHFFFAOYSA-N fenamiphos Chemical compound CCOP(=O)(NC(C)C)OC1=CC=C(SC)C(C)=C1 ZCJPOPBZHLUFHF-UHFFFAOYSA-N 0.000 abstract 1
- JFSPBVWPKOEZCB-UHFFFAOYSA-N fenfuram Chemical compound O1C=CC(C(=O)NC=2C=CC=CC=2)=C1C JFSPBVWPKOEZCB-UHFFFAOYSA-N 0.000 abstract 1
- VDLGAVXLJYLFDH-UHFFFAOYSA-N fenhexamid Chemical compound C=1C=C(O)C(Cl)=C(Cl)C=1NC(=O)C1(C)CCCCC1 VDLGAVXLJYLFDH-UHFFFAOYSA-N 0.000 abstract 1
- FKLFBQCQQYDUAM-UHFFFAOYSA-N fenpiclonil Chemical compound ClC1=CC=CC(C=2C(=CNC=2)C#N)=C1Cl FKLFBQCQQYDUAM-UHFFFAOYSA-N 0.000 abstract 1
- WHDGWKAJBYRJJL-UHFFFAOYSA-K ferbam Chemical compound [Fe+3].CN(C)C([S-])=S.CN(C)C([S-])=S.CN(C)C([S-])=S WHDGWKAJBYRJJL-UHFFFAOYSA-K 0.000 abstract 1
- GOWLARCWZRESHU-AQTBWJFISA-N ferimzone Chemical compound C=1C=CC=C(C)C=1C(/C)=N\NC1=NC(C)=CC(C)=N1 GOWLARCWZRESHU-AQTBWJFISA-N 0.000 abstract 1
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 abstract 1
- KVDJTXBXMWJJEF-UHFFFAOYSA-N fluopyram Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CCNC(=O)C1=CC=CC=C1C(F)(F)F KVDJTXBXMWJJEF-UHFFFAOYSA-N 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- GNVDAZSPJWCIQZ-UHFFFAOYSA-N flusulfamide Chemical compound ClC1=CC([N+](=O)[O-])=CC=C1NS(=O)(=O)C1=CC=C(Cl)C(C(F)(F)F)=C1 GNVDAZSPJWCIQZ-UHFFFAOYSA-N 0.000 abstract 1
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 abstract 1
- ZEYJIQLVKGBLEM-UHFFFAOYSA-N fuberidazole Chemical compound C1=COC(C=2N=C3[CH]C=CC=C3N=2)=C1 ZEYJIQLVKGBLEM-UHFFFAOYSA-N 0.000 abstract 1
- 229940097068 glyphosate Drugs 0.000 abstract 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 239000004009 herbicide Substances 0.000 abstract 1
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 abstract 1
- 229940056881 imidacloprid Drugs 0.000 abstract 1
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 abstract 1
- FCOAHACKGGIURQ-UHFFFAOYSA-N iprobenfos Chemical compound CC(C)OP(=O)(OC(C)C)SCC1=CC=CC=C1 FCOAHACKGGIURQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 abstract 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 abstract 1
- 229920000940 maneb Polymers 0.000 abstract 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052753 mercury Inorganic materials 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 abstract 1
- CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- KQUQKVGNBPTEFO-UHFFFAOYSA-L n,n-dimethylcarbamodithioate;manganese(2+) Chemical compound [Mn+2].CN(C)C([S-])=S.CN(C)C([S-])=S KQUQKVGNBPTEFO-UHFFFAOYSA-L 0.000 abstract 1
- LOBQSWSJSRZHRU-UHFFFAOYSA-N n-[2-(2-chloro-1,1,2-trifluoroethoxy)phenyl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1OC(F)(F)C(F)Cl LOBQSWSJSRZHRU-UHFFFAOYSA-N 0.000 abstract 1
- XGXNTJHZPBRBHJ-UHFFFAOYSA-N n-phenylpyrimidin-2-amine Chemical compound N=1C=CC=NC=1NC1=CC=CC=C1 XGXNTJHZPBRBHJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002018 neem oil Substances 0.000 abstract 1
- 229940049964 oleate Drugs 0.000 abstract 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 abstract 1
- 229960000321 oxolinic acid Drugs 0.000 abstract 1
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 abstract 1
- IWVCMVBTMGNXQD-PXOLEDIWSA-N oxytetracycline Chemical compound C1=CC=C2[C@](O)(C)[C@H]3[C@H](O)[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-PXOLEDIWSA-N 0.000 abstract 1
- 229960000625 oxytetracycline Drugs 0.000 abstract 1
- 235000019366 oxytetracycline Nutrition 0.000 abstract 1
- 229920002866 paraformaldehyde Polymers 0.000 abstract 1
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 abstract 1
- NAYYNDKKHOIIOD-UHFFFAOYSA-N phthalamide Chemical compound NC(=O)C1=CC=CC=C1C(N)=O NAYYNDKKHOIIOD-UHFFFAOYSA-N 0.000 abstract 1
- MGOHCFMYLBAPRN-UHFFFAOYSA-N pinoxaden Chemical compound CCC1=CC(C)=CC(CC)=C1C(C1=O)=C(OC(=O)C(C)(C)C)N2N1CCOCC2 MGOHCFMYLBAPRN-UHFFFAOYSA-N 0.000 abstract 1
- NJBFOOCLYDNZJN-UHFFFAOYSA-N pipobroman Chemical compound BrCCC(=O)N1CCN(C(=O)CCBr)CC1 NJBFOOCLYDNZJN-UHFFFAOYSA-N 0.000 abstract 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 abstract 1
- 235000015497 potassium bicarbonate Nutrition 0.000 abstract 1
- 239000011736 potassium bicarbonate Substances 0.000 abstract 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 abstract 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 abstract 1
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 abstract 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 abstract 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 abstract 1
- FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 0.000 abstract 1
- JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 abstract 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 abstract 1
- 239000001632 sodium acetate Substances 0.000 abstract 1
- 235000017454 sodium diacetate Nutrition 0.000 abstract 1
- JXKPEJDQGNYQSM-UHFFFAOYSA-M sodium propionate Chemical compound [Na+].CCC([O-])=O JXKPEJDQGNYQSM-UHFFFAOYSA-M 0.000 abstract 1
- 239000004324 sodium propionate Substances 0.000 abstract 1
- 235000010334 sodium propionate Nutrition 0.000 abstract 1
- 229960003212 sodium propionate Drugs 0.000 abstract 1
- 229960005322 streptomycin Drugs 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 229960005349 sulfur Drugs 0.000 abstract 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 abstract 1
- 239000004308 thiabendazole Substances 0.000 abstract 1
- 235000010296 thiabendazole Nutrition 0.000 abstract 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 abstract 1
- 229960004546 thiabendazole Drugs 0.000 abstract 1
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 abstract 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 abstract 1
- 239000001789 thuja occidentalis l. leaf oil Substances 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
- 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
- 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
Classifications
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Reivindicacion 1: Una composicion fungicida adecuada para el control de enfermedades causadas por fitopatogenos, que comprende: (A) un compuesto de formula 1 en donde R1 es metilo, etilo o isopropilo; R2 es 2-cloro-6-fluoro-fenilo, 2,4,6-trifluorofenilo o 2,6-difluoro-4-metoxi-fenilo; R3 es cloro, fluoro o metoxi; y (B) un compuesto seleccionado del grupo que consiste en (B1) un fungicida de estrobilurina, (B2) un fungicida de azol, (B3) un fungicida de morfolina; (B4) un fungicida de anilinopirimidina, (B5) un fungicida seleccionado del grupo que consiste en anilazina, arsenatos, benalaxilo, benalaxilo-M, benodanilo, benomilo, bentiavalicarb, bentiavalicarb-isopropilo, bifenilo, bitertanol, blasticidina-S, mezcla bordeaux, boscalid, bupirimato, cloruro de cadmio, captafol, captano, carbendazim, disulfuro de carbono, carboxina, carpropamid, aceite de hoja de cedro, chinometionato, cloro, cloroneb, clorotalonilo, clozolinato, cinamaldehído, cobre, amoniocarbonato de cobre, hidroxido de cobre, octanoato de cobre. oleato de cobre, sulfato de cobre, ciazofamid, cicloheximida, cimoxanilo, diclofluanid, diclona, dicloropropeno, diclocimet, diclomezina, dicloran, dietofencarb, diflumetorim, dimetirimol, dimetomorf, dinocap, ditianon, dodina, edifenfos, etaboxam, etirimol, etridiazol, famoxadona, fenamidona, fenaminosulf, fenamifos, fenarimol, fenfuram, fenhexamid, fenoxanilo, fenpiclonilo, acetato de fentina, cloruro de fentina, hidroxido de fentina, ferbam, ferimzona. fluazinam, fludioxonilo, flusulfamida, flutolanilo, folpet, formaldehído, fosetil-aluminio, ftalida, fuberidazol, furalaxilo. furametpir, fliodin, fuazatina, hexaclorobenceno, himexazol, iminoctadina, iodocarb, iprobenfos, iprodiona, iprovalicarb, isoprotiolano, kasugamicina, mancozeb, maneb, dimetilditiocarbamato manganoso, mefenoxam, mepronilo, cloruro mercurico, mercurio, metalaxilo, metasulfocarb, metiram, metrafenona, nabam, aceite de neem, nuarimol, octilnona, ofurace, oxadixilo, oxina de cobre, ácido oxolínico, oxicarboxina, oxitetraciclina, paclobutrazol, aceite de parafina, paraformaldehído, pencicuron, pentacloronitrobenceno, pentaclorofenol, pentiopirad, perfurazoato, ácido fosforico, polioxina, polioxina D sal de zinc, bicarbonato de potasio, probenazol, procimidona, propamocarb, propineb, proquinazid, protiocarb, pirazofos. pirifenox, piroquilon, quinoxifeno, quintozeno, siltiofam, bicarbonato de sodio, diacetato de sodio, propionato de sodio, estreptomicina, azufre, TCMTB, tecloftaIam, tecnazeno, tiabendazol, tifluzamida, tiofanato, tiofanato-metilo, tiram, tolclofos-metilo, tolilfluanid, triazoxido, tricoderma harzianio, triciclazol, triforina, hidroxido de trifenilestano, validamicina, vinclozolin, zineb, ziram, zoxamida, 1,1-bis(4-clorofenil)-2-etoxietanol, bencenosulfonato de 2,4-diclorofenilo, 2-fluoro-N-metil-N-1-naftilacetamida, 4-clorofenil-fenil sulfona, un compuesto de formula B-5.1 n compuesto de formula B-5.2, un compuesto de formula B-5.3, un compuesto de formula B-5.4, un compuesto de formula B-5.5, un compuesto de formula B-5.6, un compuesto de formula B-5.7, (2-biciclopropil-2-il-fenil)-amida del ácido 3-difluorometil-1-metil-1H-pirazol-4-carboxílico, (9-isopropip-1,2,3,4-tetrahidro-1,4-metano-naftalen-5-il)-amida del ácido 3-difluorometil-1-metil-1H-pirazol-4-carboxílico, [2-(1,3-dimetilbutil)fenil]-amida del ácido 1,3-dimetil-5-fluoro-1H-pirazol-4-carboxílico, (3'4'-dicloro-5-fluoro-1,1'-bifenil-2-il)-amida del ácido 3-difluorometil-1-metil-1H-pirazol-4-carboxílico, N-{2-[3-cloro-5-(trifluorometil)piridin-2-il]etil}-2- (trifluorometil)benzamida, N-[2-(1,1,2,2-tetrafluoroetoxi)fenil]-amida del ácido 3-difluorometil-1-metil-1H-pirazol-4-carboxílico, N-[2-(1,1,2,3,3,3-hexafluoropropoxi)fenil]-amida del ácido 3-difluorometil-1-metil-1H-pirazol-4-carboxílico, N-[2-(2-cloro-1,1,2- trifluoroetoxi)fenil]-amida del ácido 3-difluorometil-1-metil-1H-pirazol- 4-carboxílico, N-(4'-trifluorometil-bifen-2-il)-amida del ácido 3-difluorometil-1-metil-1H-pirazol-4-carboxílico, N-(2'-trifluorometil-bifen-2-il)-amida del ácido 3-difluorometil-1-metil-1H-pirazol-4-carboxílico, N-(2'-trifluorometil-bifen-2-il)-amida del ácido 3- difluorometil-1-metil-1H-pirazol-4-carboxílico, un compuesto de formula B-5.19, un compuesto de formula B-5.20, (B6) un biorregulador de plantas seleccionado del grupo que consiste en acibenzolar-S-metilo, cloruro de clormequat, etefon, cloruro de mepiquat y trinexapac-etilo; (B7) un insecticida seleccionado del grupo que consiste en abamectina, clotianidina, benzoato de emamectina, imidacloprid, teflutrina, tiametoxam, lambda cihalotrina, un compuesto de formula B-7.1, un compuesto de formula B-7.2; y (B8) un herbicida seleccionado del grupo que consiste en glifosato, clodinafop propargilo y pinoxaden. Reivindicacion 6: La composicion de acuerdo con la reivindicacion 1, en donde el componente (B) se selecciona del grupo que consiste en (B1) un fungicida de estrobilurina: azoxistrobina; (B2) un fungicida de azol seleccionado del grupo que consiste en ciproconazol, difenoconazol, epoxiconazol, propiconazol, protioconazol; (B4) un fungicida de anilino-pirimidina, ciprodinilo; (B5) un fungicida seleccionado del grupo que consiste en clorotalonilo, mancozeb y un compuesto de formula B-5.19; y (B7) un insecticida: tiametoxam. Reivindicacion 8: Un método para controlar enfermedades en plantas utiles o en su material de propagacion causadas por fitopatogenos, que comprende aplicar a las plantas utiles, a su locus o a su material de propagacion una composicion de acuerdo con la reivindicacion 1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0800760.1A GB0800760D0 (en) | 2008-01-16 | 2008-01-16 | Fungicidal compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR071332A1 true AR071332A1 (es) | 2010-06-16 |
Family
ID=39165848
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090100125A AR071332A1 (es) | 2008-01-16 | 2009-01-15 | Composiciones fungicidas |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20110142802A1 (es) |
| EP (1) | EP2229057A1 (es) |
| JP (1) | JP2011509959A (es) |
| CN (1) | CN101909445A (es) |
| AR (1) | AR071332A1 (es) |
| AU (1) | AU2009204980A1 (es) |
| CA (1) | CA2734596A1 (es) |
| GB (1) | GB0800760D0 (es) |
| WO (1) | WO2009090038A1 (es) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2008014672A (es) * | 2006-05-19 | 2009-03-09 | Abbott Lab | Derivados de alcano azabiciclico sustituidos con bicicloheterociclo fusionado activos en el sistema nervioso central. |
| WO2011095459A1 (en) | 2010-02-04 | 2011-08-11 | Syngenta Participations Ag | Pyridazine derivatives, process for their preparation and their use as fungicides |
| JP5529831B2 (ja) * | 2010-12-22 | 2014-06-25 | ダウ グローバル テクノロジーズ エルエルシー | グリホサート化合物とｉｐｂｃとの相乗的組み合わせ |
| CN102302026A (zh) * | 2011-03-12 | 2012-01-04 | 陕西汤普森生物科技有限公司 | 一种含有吡唑醚菌酯与抗生素类化合物的杀菌组合物 |
| CN102986668A (zh) * | 2011-09-18 | 2013-03-27 | 深圳诺普信农化股份有限公司 | 一种含有二氰蒽醌的杀菌组合物 |
| CN102349514A (zh) * | 2011-10-11 | 2012-02-15 | 海利尔药业集团股份有限公司 | 一种含有乙嘧酚磺酸酯的杀菌组合物 |
| CN102524274A (zh) * | 2011-12-29 | 2012-07-04 | 陕西美邦农药有限公司 | 一种含烯丙苯噻唑与三唑类的杀菌组合物 |
| WO2013127857A1 (en) * | 2012-03-01 | 2013-09-06 | Basf Se | Use of an agrochemical composition with fungicidal and plant health improving action in cereals |
| CN103371186B (zh) * | 2012-04-14 | 2017-03-08 | 中州大学 | 一种杀菌组合物 |
| CN103719098B (zh) * | 2012-10-15 | 2016-05-18 | 海利尔药业集团股份有限公司 | 一种含有乙嘧酚磺酸酯与苯醚甲环唑的杀菌组合物 |
| CN104604875A (zh) * | 2015-01-21 | 2015-05-13 | 浙江泰达作物科技有限公司 | 一种氟唑环菌胺与啶氧菌酯的杀菌组合物及其用途 |
| CN106135229A (zh) * | 2015-04-13 | 2016-11-23 | 南京华洲药业有限公司 | 一种含啶酰菌胺和噁唑菌酮的杀菌组合物及其应用 |
| CN106135208A (zh) * | 2015-04-13 | 2016-11-23 | 南京华洲药业有限公司 | 一种含啶酰菌胺和甲霜灵的杀菌组合物及其应用 |
| CN106135241A (zh) * | 2015-04-13 | 2016-11-23 | 南京华洲药业有限公司 | 一种含啶酰菌胺和多氧霉素的杀菌组合物及其应用 |
| CN106135209B (zh) * | 2015-04-13 | 2018-11-20 | 南京华洲药业有限公司 | 一种含啶酰菌胺和稻瘟酰胺的杀菌组合物及其应用 |
| CN105379754A (zh) * | 2015-12-16 | 2016-03-09 | 联保作物科技有限公司 | 一种杀虫杀菌组合物及其应用、制剂 |
| WO2017110864A1 (ja) * | 2015-12-25 | 2017-06-29 | 住友化学株式会社 | 植物病害防除組成物およびその用途 |
| CN114302646B (zh) * | 2019-06-15 | 2024-06-04 | Jdm科学研究组织私人有限公司 | 协同杀菌组合物 |
| CN110583640A (zh) * | 2019-09-30 | 2019-12-20 | 江苏七洲绿色化工股份有限公司 | 一种含有吡唑醚菌酯和苯醚甲环唑的可乳化颗粒剂及其制备方法和应用 |
| CN116530513B (zh) * | 2023-07-07 | 2023-09-15 | 中山大学 | 丙酸盐在防治柑橘黄单胞杆菌中的应用 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5092372B2 (ja) * | 2005-12-07 | 2012-12-05 | 住友化学株式会社 | ピリダジン化合物及びそれを含有する殺菌剤 |
| JP5040275B2 (ja) * | 2005-12-07 | 2012-10-03 | 住友化学株式会社 | ピリダジン化合物及びそれを有効成分として含有する植物病害防除剤 |
| GB0614153D0 (en) * | 2006-07-17 | 2006-08-23 | Syngenta Participations Ag | Novel pyridazine derivatives |
-
2008
- 2008-01-16 GB GBGB0800760.1A patent/GB0800760D0/en not_active Ceased
-
2009
- 2009-01-14 AU AU2009204980A patent/AU2009204980A1/en not_active Abandoned
- 2009-01-14 JP JP2010542574A patent/JP2011509959A/ja not_active Withdrawn
- 2009-01-14 US US12/863,372 patent/US20110142802A1/en not_active Abandoned
- 2009-01-14 WO PCT/EP2009/000165 patent/WO2009090038A1/en not_active Ceased
- 2009-01-14 CA CA2734596A patent/CA2734596A1/en not_active Abandoned
- 2009-01-14 EP EP09701512A patent/EP2229057A1/en not_active Withdrawn
- 2009-01-14 CN CN2009801023614A patent/CN101909445A/zh active Pending
- 2009-01-15 AR ARP090100125A patent/AR071332A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| GB0800760D0 (en) | 2008-02-27 |
| EP2229057A1 (en) | 2010-09-22 |
| CN101909445A (zh) | 2010-12-08 |
| AU2009204980A1 (en) | 2009-07-23 |
| JP2011509959A (ja) | 2011-03-31 |
| US20110142802A1 (en) | 2011-06-16 |
| WO2009090038A1 (en) | 2009-07-23 |
| CA2734596A1 (en) | 2009-07-23 |
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