AR117259A1 - Composiciones herbicidas - Google Patents
Composiciones herbicidasInfo
- Publication number
- AR117259A1 AR117259A1 ARP190103561A ARP190103561A AR117259A1 AR 117259 A1 AR117259 A1 AR 117259A1 AR P190103561 A ARP190103561 A AR P190103561A AR P190103561 A ARP190103561 A AR P190103561A AR 117259 A1 AR117259 A1 AR 117259A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- alkyl
- substances
- cyano
- active
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title abstract 16
- 239000004009 herbicide Substances 0.000 title abstract 3
- 239000000203 mixture Substances 0.000 title abstract 3
- 239000000126 substance Substances 0.000 abstract 9
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 4
- 125000001153 fluoro group Chemical group F* 0.000 abstract 4
- 150000002431 hydrogen Chemical class 0.000 abstract 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- 239000013543 active substance Substances 0.000 abstract 3
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 3
- -1 (7-fluoro-1H-indol-6-yl) pyridin Chemical compound 0.000 abstract 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 2
- IRJQWZWMQCVOLA-ZBKNUEDVSA-N 2-[(z)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylic acid Chemical compound N=1C=CC=C(C(O)=O)C=1C(/C)=N\NC(=O)NC1=CC(F)=CC(F)=C1 IRJQWZWMQCVOLA-ZBKNUEDVSA-N 0.000 abstract 2
- 239000005630 Diquat Substances 0.000 abstract 2
- BXEHUCNTIZGSOJ-UHFFFAOYSA-N Esprocarb Chemical compound CC(C)C(C)N(CC)C(=O)SCC1=CC=CC=C1 BXEHUCNTIZGSOJ-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- BXIGJZDQFDFASM-UHFFFAOYSA-N cyclopyrimorate Chemical compound N=1N=C(Cl)C=C(OC(=O)N2CCOCC2)C=1OC=1C(C)=CC=CC=1C1CC1 BXIGJZDQFDFASM-UHFFFAOYSA-N 0.000 abstract 2
- SYJFEGQWDCRVNX-UHFFFAOYSA-N diquat Chemical compound C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 SYJFEGQWDCRVNX-UHFFFAOYSA-N 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 abstract 2
- 239000011734 sodium Substances 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- AIAYSXFWIUNXRC-PHIMTYICSA-N (1r,5s)-3-[hydroxy-[2-(2-methoxyethoxymethyl)-6-(trifluoromethyl)pyridin-3-yl]methylidene]bicyclo[3.2.1]octane-2,4-dione Chemical compound COCCOCC1=NC(C(F)(F)F)=CC=C1C(O)=C1C(=O)[C@@H](C2)CC[C@@H]2C1=O AIAYSXFWIUNXRC-PHIMTYICSA-N 0.000 abstract 1
- ROBSGBGTWRRYSK-SNVBAGLBSA-N (2r)-2-[4-(4-cyano-2-fluorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=CC=C(C#N)C=C1F ROBSGBGTWRRYSK-SNVBAGLBSA-N 0.000 abstract 1
- 125000006592 (C2-C3) alkenyl group Chemical group 0.000 abstract 1
- 125000006593 (C2-C3) alkynyl group Chemical group 0.000 abstract 1
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 abstract 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 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
- WVQBLGZPHOPPFO-LBPRGKRZSA-N (S)-metolachlor Chemical compound CCC1=CC=CC(C)=C1N([C@@H](C)COC)C(=O)CCl WVQBLGZPHOPPFO-LBPRGKRZSA-N 0.000 abstract 1
- XUHGTGGPZFJRMF-UHFFFAOYSA-N 1,3-dihydropyrazole-2-carboxylic acid Chemical compound OC(=O)N1CC=CN1 XUHGTGGPZFJRMF-UHFFFAOYSA-N 0.000 abstract 1
- DHYXNIKICPUXJI-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-n-(2,4-difluorophenyl)-5-oxo-n-propan-2-yl-1,2,4-triazole-4-carboxamide Chemical compound C=1C=C(F)C=C(F)C=1N(C(C)C)C(=O)N(C1=O)C=NN1C1=CC=C(Cl)C=C1Cl DHYXNIKICPUXJI-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
- GHLCSCRDVVEUQD-UHFFFAOYSA-N 1-({1-ethyl-4-[3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoyl]-1H-pyrazol-5-yl}oxy)ethyl methyl carbonate Chemical compound CCN1N=CC(C(=O)C=2C(=C(OCCOC)C(=CC=2)S(C)(=O)=O)C)=C1OC(C)OC(=O)OC GHLCSCRDVVEUQD-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
- 239000002794 2,4-DB Substances 0.000 abstract 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 abstract 1
- KGKGSIUWJCAFPX-UHFFFAOYSA-N 2,6-dichlorothiobenzamide Chemical compound NC(=S)C1=C(Cl)C=CC=C1Cl KGKGSIUWJCAFPX-UHFFFAOYSA-N 0.000 abstract 1
- BDQWWOHKFDSADC-UHFFFAOYSA-N 2-(2,4-dichloro-3-methylphenoxy)-n-phenylpropanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C)OC1=CC=C(Cl)C(C)=C1Cl BDQWWOHKFDSADC-UHFFFAOYSA-N 0.000 abstract 1
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 abstract 1
- NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 abstract 1
- YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 abstract 1
- MAYMYMXYWIVVOK-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-4-(methanesulfonamidomethyl)benzoic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(CNS(C)(=O)=O)C=2)C(O)=O)=N1 MAYMYMXYWIVVOK-UHFFFAOYSA-N 0.000 abstract 1
- HCNBYBFTNHEQQJ-UHFFFAOYSA-N 2-[(4,6-dimethoxypyrimidin-2-yl)carbamoylsulfamoyl]-6-(trifluoromethyl)pyridine-3-carboxylic acid Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(N=2)C(F)(F)F)C(O)=O)=N1 HCNBYBFTNHEQQJ-UHFFFAOYSA-N 0.000 abstract 1
- UWHURBUBIHUHSU-UHFFFAOYSA-N 2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 UWHURBUBIHUHSU-UHFFFAOYSA-N 0.000 abstract 1
- KRQUFUKTQHISJB-YYADALCUSA-N 2-[(E)-N-[2-(4-chlorophenoxy)propoxy]-C-propylcarbonimidoyl]-3-hydroxy-5-(thian-3-yl)cyclohex-2-en-1-one Chemical compound CCC\C(=N/OCC(C)OC1=CC=C(Cl)C=C1)C1=C(O)CC(CC1=O)C1CCCSC1 KRQUFUKTQHISJB-YYADALCUSA-N 0.000 abstract 1
- GQQIAHNFBAFBCS-UHFFFAOYSA-N 2-[2-chloro-5-(1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)-4-fluorophenoxy]acetic acid Chemical compound C1=C(Cl)C(OCC(=O)O)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1F GQQIAHNFBAFBCS-UHFFFAOYSA-N 0.000 abstract 1
- OOLBCHYXZDXLDS-UHFFFAOYSA-N 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1Cl OOLBCHYXZDXLDS-UHFFFAOYSA-N 0.000 abstract 1
- MPPOHAUSNPTFAJ-UHFFFAOYSA-N 2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 MPPOHAUSNPTFAJ-UHFFFAOYSA-N 0.000 abstract 1
- CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 abstract 1
- IOYNQIMAUDJVEI-ZFNPBRLTSA-N 2-[N-[(E)-3-chloroprop-2-enoxy]-C-ethylcarbonimidoyl]-3-hydroxy-5-(oxan-4-yl)cyclohex-2-en-1-one Chemical compound C1C(=O)C(C(=NOC\C=C\Cl)CC)=C(O)CC1C1CCOCC1 IOYNQIMAUDJVEI-ZFNPBRLTSA-N 0.000 abstract 1
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 abstract 1
- YHKBGVDUSSWOAB-UHFFFAOYSA-N 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoic acid Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(CC(Cl)C(O)=O)=C(Cl)C=C1F YHKBGVDUSSWOAB-UHFFFAOYSA-N 0.000 abstract 1
- JLYFCTQDENRSOL-UHFFFAOYSA-N 2-chloro-N-(2,4-dimethylthiophen-3-yl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound COCC(C)N(C(=O)CCl)C=1C(C)=CSC=1C JLYFCTQDENRSOL-UHFFFAOYSA-N 0.000 abstract 1
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 abstract 1
- KZNDFYDURHAESM-UHFFFAOYSA-N 2-chloro-n-(2-ethyl-6-methylphenyl)-n-(propan-2-yloxymethyl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(COC(C)C)C(=O)CCl KZNDFYDURHAESM-UHFFFAOYSA-N 0.000 abstract 1
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 abstract 1
- UFAPVJDEYHLLBG-UHFFFAOYSA-N 2-{2-chloro-4-(methylsulfonyl)-3-[(tetrahydrofuran-2-ylmethoxy)methyl]benzoyl}cyclohexane-1,3-dione Chemical compound ClC1=C(COCC2OCCC2)C(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O UFAPVJDEYHLLBG-UHFFFAOYSA-N 0.000 abstract 1
- ABOOPXYCKNFDNJ-UHFFFAOYSA-N 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-UHFFFAOYSA-N 0.000 abstract 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 abstract 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 abstract 1
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 abstract 1
- CASLETQIYIQFTQ-UHFFFAOYSA-N 3-[[5-(difluoromethoxy)-1-methyl-3-(trifluoromethyl)pyrazol-4-yl]methylsulfonyl]-5,5-dimethyl-4h-1,2-oxazole Chemical compound CN1N=C(C(F)(F)F)C(CS(=O)(=O)C=2CC(C)(C)ON=2)=C1OC(F)F CASLETQIYIQFTQ-UHFFFAOYSA-N 0.000 abstract 1
- MBFHUWCOCCICOK-UHFFFAOYSA-N 4-iodo-2-[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoylsulfamoyl]benzoic acid Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=C(I)C=2)C(O)=O)=N1 MBFHUWCOCCICOK-UHFFFAOYSA-N 0.000 abstract 1
- NYRMIJKDBAQCHC-UHFFFAOYSA-N 5-(methylamino)-2-phenyl-4-[3-(trifluoromethyl)phenyl]furan-3(2H)-one Chemical compound O1C(NC)=C(C=2C=C(C=CC=2)C(F)(F)F)C(=O)C1C1=CC=CC=C1 NYRMIJKDBAQCHC-UHFFFAOYSA-N 0.000 abstract 1
- QQOGZMUZAZWLJH-UHFFFAOYSA-N 5-[2-chloro-6-fluoro-4-(trifluoromethyl)phenoxy]-n-ethylsulfonyl-2-nitrobenzamide Chemical compound C1=C([N+]([O-])=O)C(C(=O)NS(=O)(=O)CC)=CC(OC=2C(=CC(=CC=2F)C(F)(F)F)Cl)=C1 QQOGZMUZAZWLJH-UHFFFAOYSA-N 0.000 abstract 1
- CTSLUCNDVMMDHG-UHFFFAOYSA-N 5-bromo-3-(butan-2-yl)-6-methylpyrimidine-2,4(1H,3H)-dione Chemical compound CCC(C)N1C(=O)NC(C)=C(Br)C1=O CTSLUCNDVMMDHG-UHFFFAOYSA-N 0.000 abstract 1
- PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 abstract 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 abstract 1
- 239000002890 Aclonifen Substances 0.000 abstract 1
- XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 abstract 1
- 239000003666 Amidosulfuron Substances 0.000 abstract 1
- CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 abstract 1
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 abstract 1
- NXQDBZGWYSEGFL-UHFFFAOYSA-N Anilofos Chemical compound COP(=S)(OC)SCC(=O)N(C(C)C)C1=CC=C(Cl)C=C1 NXQDBZGWYSEGFL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005469 Azimsulfuron Substances 0.000 abstract 1
- 239000005471 Benfluralin Substances 0.000 abstract 1
- 239000005476 Bentazone Substances 0.000 abstract 1
- JDWQITFHZOBBFE-UHFFFAOYSA-N Benzofenap Chemical compound C=1C=C(Cl)C(C)=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=C(C)C=C1 JDWQITFHZOBBFE-UHFFFAOYSA-N 0.000 abstract 1
- 239000005484 Bifenox Substances 0.000 abstract 1
- XTFNPKDYCLFGPV-OMCISZLKSA-N Bromofenoxim Chemical compound C1=C(Br)C(O)=C(Br)C=C1\C=N\OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O XTFNPKDYCLFGPV-OMCISZLKSA-N 0.000 abstract 1
- 239000005489 Bromoxynil Substances 0.000 abstract 1
- OEYOMNZEMCPTKN-UHFFFAOYSA-N Butamifos Chemical compound CCC(C)NP(=S)(OCC)OC1=CC(C)=CC=C1[N+]([O-])=O OEYOMNZEMCPTKN-UHFFFAOYSA-N 0.000 abstract 1
- SPNQRCTZKIBOAX-UHFFFAOYSA-N Butralin Chemical compound CCC(C)NC1=C([N+]([O-])=O)C=C(C(C)(C)C)C=C1[N+]([O-])=O SPNQRCTZKIBOAX-UHFFFAOYSA-N 0.000 abstract 1
- ZOGDSYNXUXQGHF-XIEYBQDHSA-N Butroxydim Chemical compound CCCC(=O)C1=C(C)C=C(C)C(C2CC(=O)C(\C(CC)=N\OCC)=C(O)C2)=C1C ZOGDSYNXUXQGHF-XIEYBQDHSA-N 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 239000005490 Carbetamide Substances 0.000 abstract 1
- HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 abstract 1
- NLYNUTMZTCLNOO-UHFFFAOYSA-N Chlorbromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C(Cl)=C1 NLYNUTMZTCLNOO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005647 Chlorpropham Substances 0.000 abstract 1
- 241000723347 Cinnamomum Species 0.000 abstract 1
- WMLPCIHUFDKWJU-UHFFFAOYSA-N Cinosulfuron Chemical compound COCCOC1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC)=NC(OC)=N1 WMLPCIHUFDKWJU-UHFFFAOYSA-N 0.000 abstract 1
- 239000005497 Clethodim Substances 0.000 abstract 1
- 239000005499 Clomazone Substances 0.000 abstract 1
- OFSLKOLYLQSJPB-UHFFFAOYSA-N Cyclosulfamuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)NC=2C(=CC=CC=2)C(=O)C2CC2)=N1 OFSLKOLYLQSJPB-UHFFFAOYSA-N 0.000 abstract 1
- 239000005501 Cycloxydim Substances 0.000 abstract 1
- NPOJQCVWMSKXDN-UHFFFAOYSA-N Dacthal Chemical compound COC(=O)C1=C(Cl)C(Cl)=C(C(=O)OC)C(Cl)=C1Cl NPOJQCVWMSKXDN-UHFFFAOYSA-N 0.000 abstract 1
- NNYRZQHKCHEXSD-UHFFFAOYSA-N Daimuron Chemical compound C1=CC(C)=CC=C1NC(=O)NC(C)(C)C1=CC=CC=C1 NNYRZQHKCHEXSD-UHFFFAOYSA-N 0.000 abstract 1
- 239000005503 Desmedipham Substances 0.000 abstract 1
- 239000005504 Dicamba Substances 0.000 abstract 1
- 239000005506 Diclofop Substances 0.000 abstract 1
- QNXAVFXEJCPCJO-UHFFFAOYSA-N Diclosulam Chemical compound N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1Cl QNXAVFXEJCPCJO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005507 Diflufenican Substances 0.000 abstract 1
- DHWRNDJOGMTCPB-UHFFFAOYSA-N Dimefuron Chemical compound ClC1=CC(NC(=O)N(C)C)=CC=C1N1C(=O)OC(C(C)(C)C)=N1 DHWRNDJOGMTCPB-UHFFFAOYSA-N 0.000 abstract 1
- 239000005508 Dimethachlor Substances 0.000 abstract 1
- OFDYMSKSGFSLLM-UHFFFAOYSA-N Dinitramine Chemical compound CCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C(N)=C1[N+]([O-])=O OFDYMSKSGFSLLM-UHFFFAOYSA-N 0.000 abstract 1
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- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 abstract 1
- 229940097068 glyphosate Drugs 0.000 abstract 1
- KKLBEFSLWYDQFI-UHFFFAOYSA-N halauxifen Chemical compound COC1=C(Cl)C=CC(C=2N=C(C(Cl)=C(N)C=2)C(O)=O)=C1F KKLBEFSLWYDQFI-UHFFFAOYSA-N 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- YFONKFDEZLYQDH-BOURZNODSA-N indaziflam Chemical compound CC(F)C1=NC(N)=NC(N[C@H]2C3=CC(C)=CC=C3C[C@@H]2C)=N1 YFONKFDEZLYQDH-BOURZNODSA-N 0.000 abstract 1
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- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
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- CWKFPEBMTGKLKX-UHFFFAOYSA-N picolinafen Chemical compound C1=CC(F)=CC=C1NC(=O)C1=CC=CC(OC=2C=C(C=CC=2)C(F)(F)F)=N1 CWKFPEBMTGKLKX-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
- ISEUFVQQFVOBCY-UHFFFAOYSA-N prometon Chemical compound COC1=NC(NC(C)C)=NC(NC(C)C)=N1 ISEUFVQQFVOBCY-UHFFFAOYSA-N 0.000 abstract 1
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 abstract 1
- FKLQIONHGSFYJY-UHFFFAOYSA-N propan-2-yl 5-[4-bromo-1-methyl-5-(trifluoromethyl)pyrazol-3-yl]-2-chloro-4-fluorobenzoate Chemical compound C1=C(Cl)C(C(=O)OC(C)C)=CC(C=2C(=C(N(C)N=2)C(F)(F)F)Br)=C1F FKLQIONHGSFYJY-UHFFFAOYSA-N 0.000 abstract 1
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 abstract 1
- FROBCXTULYFHEJ-OAHLLOKOSA-N propaquizafop Chemical compound C1=CC(O[C@H](C)C(=O)OCCON=C(C)C)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 FROBCXTULYFHEJ-OAHLLOKOSA-N 0.000 abstract 1
- WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 abstract 1
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 abstract 1
- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 abstract 1
- FKERUJTUOYLBKB-UHFFFAOYSA-N pyrazoxyfen Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=CC=C1 FKERUJTUOYLBKB-UHFFFAOYSA-N 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 abstract 1
- ALZOLUNSQWINIR-UHFFFAOYSA-N quinmerac Chemical compound OC(=O)C1=C(Cl)C=CC2=CC(C)=CN=C21 ALZOLUNSQWINIR-UHFFFAOYSA-N 0.000 abstract 1
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- GNHDVXLWBQYPJE-UHFFFAOYSA-N saflufenacil Chemical compound C1=C(Cl)C(C(=O)NS(=O)(=O)N(C)C(C)C)=CC(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)=C1F GNHDVXLWBQYPJE-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 abstract 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 abstract 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 1
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 abstract 1
- FZMKKCQHDROFNI-UHFFFAOYSA-N sulfometuron Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 FZMKKCQHDROFNI-UHFFFAOYSA-N 0.000 abstract 1
- 229940124530 sulfonamide Drugs 0.000 abstract 1
- 150000003456 sulfonamides Chemical class 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 abstract 1
- BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 abstract 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 abstract 1
- GLDAZAQRGCSFNP-UHFFFAOYSA-N thiencarbazone Chemical compound O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=C(C)SC=C1C(O)=O GLDAZAQRGCSFNP-UHFFFAOYSA-N 0.000 abstract 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 abstract 1
- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 abstract 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 abstract 1
- 150000003918 triazines Chemical class 0.000 abstract 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 abstract 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-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
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-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
- 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
- 150000003672 ureas Chemical class 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
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
Reivindicación 1: Composiciones que comprenden los compuestos activos herbicidas (A) y (B) caracterizadas porque (A) representa uno o más compuestos de la fórmula general (1) o sus sales aceptables para uso agroquímico [herbicida (A)], donde R¹ y R² en cada caso representan hidrógeno; R³ representa en cada caso C₁₋₃-alquilo, C₃₋₄-cicloalquilo, C₂₋₃-alquenilo, C₂₋₃-alquinilo o C₁₋₃-alcoxi sustituido con m residuos del grupo que comprende fluoro, cloro, ciano y C₁₋₂-alcoxi; Z representa un grupo Z-1, Z-2, Z-8, Z-9, Z-11 o Z-13, donde Z-1, Z2, Z-8, Z-9, Z-11 y Z-13 tienen los significados: del grupo de fórmulas (2), donde cada flecha representa un enlace al grupo C=O de la fórmula (1); R¹¹, R¹² representan en forma independiente entre sí hidrógeno, ciano, OR⁷, S(O)ₙR⁵, SO₂NR⁶R⁷, CO₂R⁸, CONR⁶R⁸, COR⁶, NR⁶R⁸, NR⁶COR⁸, NR⁶SO₂R⁸, o representan en cada caso C₁₋₆-alquilo, C₃₋₆-cicloalquilo, C₃₋₆-cicloalquil-C₁₋₃-alquilo, C₂₋₆-alquenilo, C₅₋₆-cicloalquenilo o C₂₋₆-alquinilo opcionalmente sustituido con m residuos del grupo que comprende halógeno, ciano, OR⁷, S(O)ₙR⁵, CO₂R⁸, NR⁶SO₂R⁸, o R¹¹ y R¹² junto con el átomo de nitrógeno al cual están unidos forman un anillo saturado, parcialmente insaturado o totalmente insaturado de cinco, seis o siete miembros, opcionalmente sustituido con entre uno y seis residuos del grupo que comprende halógeno, ciano, C₁₋₆-alquilo, halógeno-C₁₋₆-alquilo, oxo, OR⁷, S(O)ₙR⁵, SO₂NR⁶R⁷, CO₂R⁸, CONR⁶R⁸, que además de este átomo de nitrógeno contiene r átomos de carbono, n átomos de oxígeno, p átomos de azufre y p elementos del grupo que comprende NR⁷ y NCOR⁷ como átomos del anillo; X², X⁴ y X⁶ en forma independiente entre sí representan hidrógeno o fluoro; X³ y X⁵ representan en forma independiente entre sí hidrógeno, fluoro, cloro o ciano, o representan en cada caso C₁₋₃-alquilo o C₁₋₃-alcoxi sustituido con m residuos del grupo que comprende fluoro y cloro; R⁵ representa en cada caso C₁₋₆-alquilo, C₃₋₆-cicloalquilo o arilo sustituido con m residuos del grupo que comprende halógeno y ciano; R⁶ representa hidrógeno o R⁵; R⁷ representa hidrógeno, o representa en cada caso C₁₋₆-alquilo, C₃₋₆-cicloalquilo, C₃₋₄-alquenilo o C₃₋₄-alquinilo sustituido con m residuos del grupo que comprende halógeno, ciano y C₁₋₂-alcoxi; R⁸ representa hidrógeno, o representa en cada caso C₁₋₆-alquilo, C₃₋₆-cicloalquilo, C₃₋₆-alquenilo o C₃₋₆-alquinilo sustituido con m residuos del grupo que comprende halógeno, ciano y C₁₋₂-alcoxi; m representa el número entero 0, 1, 2 ó 3; n representa el número entero 0, 1 ó 2; p representa el número entero 0 ó 1; y r representa el número entero 3, 4, 5 ó 6; y (B) representa uno o más herbicidas [componente (B)] del grupo de las sustancias activas herbicidas (B1) hasta (B11), donde (B1) representa sustancias activas herbicidas del grupo de los compuestos 1,3-dicetona, seleccionadas entre (B1.1) Aloxidim, (B1.2) Biciclopirona, (B1.3) Butroxidim, (B1.4) Cletodim, (B1.5) Cicloxidim, (B1.6) Fenquinotriona, (B1.7) Mesotriona, (B1.8) Pinoxaden, (B1.9) Profoxidim, (B1.10) Setoxidim, (B1.11) Sulcotriona, (B1.12) SYP-9121, (B1.13) Tefuriltriona, (B1.14) Tembotriona, (B1.15) Tepraloxidim, (B1.16) Tralcoxidim, (B1.17) Y13161, (B1.18) Y13287; (B2) representa sustancias activas herbicidas del grupo de las sulfonamidas, seleccionadas entre (B2.1) Acetoclor, (B2.2) Alaclor, (B2.3) Amidosulfuron, (B2.4) Asulam, (B2.5) Azimsulfuron, (B2.6) Beflubutamida, (B2.7) Bensulfuron, (B2.8) Butaclor, (B2.9) Carbetamida, (B2.10) Clorimuron, (B2.11) Cloroprofam, (B2.12) Clorsulfuron, (B2.13) Cinosulfuron, (B2.14) Cloransulam, (B2.15) Ciclosulfamuron, (B2.16) Desmedifam, (B2.17) Diclosulam, (B2.18) Diflufenican, (B2.19) Dimetaclor, (B2.20) Dimetenamida, (B2.21) Esprocarb, (B2.22) Etametsulfuron, (B2.23) Etoxisulfuron, (B2.24) Flazasulfuron, (B2.25) Florasulam, (B2.26) Flucarbazona, (B2.27) Flucetosulfuron, (B2.28) Flufenacet, (B2.29) Flumetsulam, (B2.30) Flupirsulfuron, (B2.31) Foramsulfuron, (B2.32) Halosulfuron, (B2.33) Imazosulfuron, (B2.34) Iodosulfuron, (B2.35) Ipfencarbazona, (B2.36) Mefenacet, (B2.37) Mesosulfuron, (B2.38) Metazaclor, (B2.39) Metazosulfuron, (B2.40) Metolaclor, (B2.41) Metosulam, (B2.42) Metsulfuron, (B2.43) Nicosulfuron, (B2.44) Ortosulfamuron, (B2.45) Oxasulfuron, (B2.46) Penoxsulam, (B2.47) Petoxamida, (B2.48) Fenmedifam, (B2.49) Picolinafen, (B2.50) Pretilaclor, (B2.51) Primisulfuron, (B2.52) Propaclor, (B2.53) Propanil, (B2.54) Profam, (B2.55) Propisoclor, (B2.56) Propoxicarbazona, (B2.57) Propirisulfuron, (B2.58) Propizamida, (B2.59) Prosulfocarb, (B2.60) Prosulfuron, (B2.61) Pirazosulfuron, (B2.62) Piroxsulam, (B2.63) Rimsulfuron, (B2.64) S-metolaclor, (B2.65) Sulfometuron, (B2.66) Sulfosulfuron, (B2.67) Tenilclor, (B2.68) Tiencarbazona, (B2.69) Tifensulfuron, (B2.70) Trialato (B2.71) Triasulfuron, (B2.72) Tribenuron, (B2.73) Trifloxisulfuron, (B2.74) Triflusulfuron, (B2.75) Tritosulfuron, (B2.76) Esprocarb, (B2.77) Profluazol, (B2.78) Trialato; (B3) representa sustancias activas herbicidas del grupo de los arilnitrilos, seleccionadas entre (B3.1) Bromoxinil, (B3.2) Clorotiamida, (B3.3) Diclobenil, (B3.4) Ioxinil, (B3.5) Piraclonil; (B4) representa sustancias activas herbicidas del grupo de los azoles, seleccionadas entre (B4.1) Amicarbazona, (B4.2) Amitrol, (B4.3) Azafenidin, (B4.4) Benzofenap, (B4.5) Benzuofucaotong (B4.6) Biscarfentrazona (B4.7) Cafenstrol, (B4.8) Carfentrazona, (B4.9) Fentrazamida, (B4.10) Imazametabenz, (B4.11) Imazamox, (B4.12) Imazapic, (B4.13) Imazapir, (B4.14) Imazaquin, (B4.15) Imazetapir, (B4.16) Isouron, (B4.17) Isoxaben, (B4.18) Isoxaflutol, (B4.19) Oxadiargilo, (B4.20) Oxadiazon, (B4.21) Piraflufen, (B4.22) Pirasulfotol, (B4.23) Pirazolinato, (B4.24) Pirazoxifen, (B4.25) Piroxasulfona, (B4.26) Sulfentrazona, (B4.27) Tolpiralato, (B4.28) Topramezona (B4.29) Triazolsulcotriona (QYR301), (B4.30) QYM-201, (B4.31) Bencarbazona, (B4.32) Fluazolato, (B4.33) Flupoxam, (B4.34) Isoxaclortol; (B5) representa otras sustancias activas herbicidas, seleccionadas entre (B5.1) Aminociclopiraclor, (B5.2) Aminopiralid, (B5.3) Benazolin-etilo, (B5.4) Benfluralina, (B5.5) Bentazona, (B5.6) Benzobiciclon, (B5.7) Bixlozona (B5.8) Bromofenoxim, (B5.9) Butralina, (B5.10) Cloroidazon / Pirazon, (B5.11) Clorotal, (B5.12) Cinidon-etilo, (B5.13) Cinmetilina, (B5.14) Clomazona, (B5.15) Ciclopirimorat (B5.16) Dinitramina, (B5.17) Diquat, (B5.18) Ditiopir, (B5.19) Ácido acético, (B5.20) Etalfluralina, (B5.21) Etofumesato, (B5.22) Flamprop, (B5.23) Florpirauxifen, (B5.24) Flufenpir, (B5.25) Flumiclorac, (B5.26) Flumioxazina, (B5.27) Fluridona, (B5.28) Flurocloridona, (B5.29) Flurtamona, (B5.30) Flutiacet-metilo, (B5.31) Halauxifen, (B5.32) Indanofan, (B5.33) Norflurazon, (B5.34) Ácido oleico (B5.35) Orizalina, (B5.36) Oxaziclomefona, (B5.37) Paraquat, (B5.38) Ácido nonanoico, (B5.39) Pendimetalina, (B5.40) Pentoxazona, (B5.41) Piridafol, (B5.42) Piridato, (B5.43) Tetflupirolimet, (B5.44) Tiazopir, (B5.45) Triafamona, (B5.46) Trifluralina, (B5.47) Ácido 4-amino-3-cloro-5-fluoro-6-(7-fluoro-1H-indol-6-il)piridin-2-carboxílico, (B5.48) Ciclopirimorato, (B5.49) Diquat, (B5.50) Oxaziclomefona, (B5.51) Pentanoclor, (B5.52) Tebutam, (B5.53) Tidiazimin; (B6) representa sustancias activas herbicidas del grupo de los ácidos (het)arilcarboxílicos, seleccionadas entre (B6.1) Cloramben, (B6.2) Clopiralida, (B6.3) Dicamba, (B6.4) Fluroxipir, (B6.5) Picloram, (B6.6) Quinclorac, (B6.7) Quinmerac, (B6.8) TBA, (B6.9) Triclopir; (B7) representa sustancias activas herbicidas del grupo de los compuestos orgánicos de fósforo, seleccionadas entre (B7.1) Anilofos, (B7.2) Bialafos, (B7.3) Butamifos, (B7.4) Glufosinato, (B7.5) Glifosato, (B7.6) Piperofos, (B7.7) Sulfosato, (B7.8) Amiprofos; (B8) representa sustancias activas herbicidas del grupo de los feniléteres, seleccionadas entre (B8.1) 2,4-D, (B8.2) 2,4-DB, (B8.3) 2,4-DP, (B8.4) Acifluorfen, (B8.5) Aclonifen, (B8.6) Bifenox, (B8.7) Clometoxifen, (B8.8) Clodinafoppropargilo, (B8.9) Clomeprop, (B8.10) Cihalofop, (B8.11) Diclofop, (B8.12) Etoxifen, (B8.13) Fenoxaprop, (B8.14) Fluazifop, (B8.15) Fluoroglicofen, (B8.16) Fomesafen, (B8.17) Halosafen, (B8.18) Haloxifop, (B8.19) Lactofen, (B8.20) MCPA, (B8.21) MCPB, (B8.22) Mecoprop, (B8.23) Metamifop, (B8.24) Oxifluorfen, (B8.25) Propaquizafop, (B8.26) Quizalofop, (B8.27) Quizalofop-p, (B8.28) Benzfendizona; (B9) representa sustancias activas herbicidas del grupo de las pirimidinas, seleccionadas entre (B9.1) Bispirac-sodio, (B9.2) Bromacil, (B9.3) Butafenacil, (B9.4) Lenacil, (B9.5) Piribenzoxim, (B9.6) Piriftalid, (B9.7) Piriminobac, (B9.8) Pirimisulfan, (B9.9) Piritiobac-sodio, (B9.10) Saflufenacil, (B9.11) Terbacil, (B9.12) Tiafenacil, (B9.13) Trifludimoxazin (B9.14) [3-[2-cloro-4-fluoro-5-(1-metil-6-trifluorometil-2,4-dioxo-1,2,3,4-tetrahidropirimidin-3-il)fenoxi]-2-piridiloxi]acetato de etilo; (B10) representa sustancias activas herbicidas del grupo de las (tio)ureas, seleccionadas entre (B10.1) Clorbromuron, (B10.2) Clortoluron, (B10.3) Daimuron, (B10.4) Dimefuron, (B10.5) Diuron, (B10.6) Diflufenzopir (B10.7) Fluometuron, (B10.8) Isoproturon, (B10.9) Linuron, (B10.10) Metabenztiazuron, (B10.11) Metobromuron, (B10.12) Metoxuron, (B10.13) Monolinuron, (B10.14) Neburon, (B10.15) Siduron, (B10.16) Tebutiuron, (B10.17) Fenuron, (B10.18) Cloroxuron, (B10.19) Diflufenzopir, (B10.20) Etidimuron; (B11) representa sustancias activas herbicidas del grupo de las triazinas, seleccionadas entre (B11.1) Ametrina, (B11.2) Atrazina, (B11.3) Cinazina, (B11.4) Dimetametrina, (B11.5) Hexazinona, (B11.6) Indaziflam, (B11.7) Metamitron, (B11.8) Metribuzina, (B11.9) Prometon, (B11.10) Prometrina, (B11.11) Propazina, (B11.12) Simazina, (B11.13) Simetrina, (B11.14) Terbumeton, (B11.15) Terbutilazina, (B11.16) Terbutrina, (B11.17) Triaziflam, (B11.18) Trietazina, (B11.19) Desmetrina. Reivindicación 5: Una composición herbicida de acuerdo con una de las reivindicaciones 1 a 4, caracterizada porque los componentes activos (A) y (B) se encuentran en una relación en peso desde 1:100000 hasta 2000:1.
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| HRP20250098T1 (hr) * | 2019-07-04 | 2025-03-28 | Bayer Aktiengesellschaft | Herbicidni pripravci |
| BR112022024547A2 (pt) * | 2020-06-02 | 2022-12-27 | Bayer Ag | Herbicidas seletivos à base de carboxamidas de isoxa-zolina substituidas e de furilazol |
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-
2019
- 2019-12-02 UA UAA202103960A patent/UA129356C2/uk unknown
- 2019-12-02 CA CA3122157A patent/CA3122157A1/en active Pending
- 2019-12-02 JP JP2021531710A patent/JP7657715B2/ja active Active
- 2019-12-02 EP EP19809102.7A patent/EP3890489B1/de active Active
- 2019-12-02 ES ES19809102T patent/ES2942215T3/es active Active
- 2019-12-02 EA EA202191568A patent/EA202191568A1/ru unknown
- 2019-12-02 MX MX2021006669A patent/MX2021006669A/es unknown
- 2019-12-02 CN CN201980089747.XA patent/CN113329630B/zh active Active
- 2019-12-02 PL PL19809102.7T patent/PL3890489T3/pl unknown
- 2019-12-02 KR KR1020217020763A patent/KR102834126B1/ko active Active
- 2019-12-02 AU AU2019393950A patent/AU2019393950B2/en active Active
- 2019-12-02 WO PCT/EP2019/083228 patent/WO2020114934A1/de not_active Ceased
- 2019-12-02 MY MYPI2021003066A patent/MY202868A/en unknown
- 2019-12-02 BR BR112021009734-1A patent/BR112021009734B1/pt active IP Right Grant
- 2019-12-02 US US17/299,709 patent/US20220053762A1/en not_active Abandoned
- 2019-12-05 AR ARP190103561A patent/AR117259A1/es active IP Right Grant
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2021
- 2021-06-03 CL CL2021001467A patent/CL2021001467A1/es unknown
- 2021-06-07 PH PH12021551338A patent/PH12021551338A1/en unknown
- 2021-07-06 ZA ZA2021/04714A patent/ZA202104714B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CL2021001467A1 (es) | 2021-11-19 |
| KR102834126B1 (ko) | 2025-07-15 |
| EP3890489B1 (de) | 2023-01-04 |
| PL3890489T3 (pl) | 2023-05-08 |
| EA202191568A1 (ru) | 2021-10-28 |
| CN113329630A (zh) | 2021-08-31 |
| KR20210102296A (ko) | 2021-08-19 |
| ZA202104714B (en) | 2024-12-18 |
| ES2942215T3 (es) | 2023-05-30 |
| BR112021009734A2 (pt) | 2021-08-17 |
| AU2019393950B2 (en) | 2025-06-26 |
| EP3890489A1 (de) | 2021-10-13 |
| CA3122157A1 (en) | 2020-06-11 |
| BR112021009734B1 (pt) | 2023-12-19 |
| JP2022511488A (ja) | 2022-01-31 |
| PH12021551338A1 (en) | 2021-12-13 |
| CN113329630B (zh) | 2024-04-26 |
| MY202868A (en) | 2024-05-27 |
| JP7657715B2 (ja) | 2025-04-07 |
| US20220053762A1 (en) | 2022-02-24 |
| UA129356C2 (uk) | 2025-03-26 |
| MX2021006669A (es) | 2021-07-07 |
| WO2020114934A1 (de) | 2020-06-11 |
| AU2019393950A1 (en) | 2021-06-24 |
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