AR035286A1 - Herbicidas selectivos que contienen un derivado de tetrazolinona. - Google Patents
Herbicidas selectivos que contienen un derivado de tetrazolinona.Info
- Publication number
- AR035286A1 AR035286A1 ARP020103126A ARP020103126A AR035286A1 AR 035286 A1 AR035286 A1 AR 035286A1 AR P020103126 A ARP020103126 A AR P020103126A AR P020103126 A ARP020103126 A AR P020103126A AR 035286 A1 AR035286 A1 AR 035286A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- chloro
- alkyl
- phenyl
- halogen
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 3
- JXBKZAYVMSNKHA-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-olate Chemical class OC=1N=NNN=1 JXBKZAYVMSNKHA-UHFFFAOYSA-N 0.000 title abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 9
- -1 4,6-dimethoxy-2-pyrimidinyl Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 7
- 150000001875 compounds Chemical class 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 5
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 5
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 3
- MCNOFYBITGAAGM-UHFFFAOYSA-N 2,2-dichloro-1-[5-(furan-2-yl)-2,2-dimethyl-1,3-oxazolidin-3-yl]ethanone Chemical compound C1N(C(=O)C(Cl)Cl)C(C)(C)OC1C1=CC=CO1 MCNOFYBITGAAGM-UHFFFAOYSA-N 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004414 alkyl thio group Chemical group 0.000 abstract 3
- 150000002431 hydrogen Chemical class 0.000 abstract 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 159000000000 sodium salts Chemical class 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 2
- 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 2
- MHULQDZDXMHODA-UHFFFAOYSA-N 1-(2,2-dichloroacetyl)-3,3,8a-trimethyl-2,4,7,8-tetrahydropyrrolo[1,2-a]pyrimidin-6-one Chemical compound C1C(C)(C)CN(C(=O)C(Cl)Cl)C2(C)N1C(=O)CC2 MHULQDZDXMHODA-UHFFFAOYSA-N 0.000 abstract 2
- QWWHRELOCZEQNZ-UHFFFAOYSA-N 2,2-dichloro-1-(1-oxa-4-azaspiro[4.5]decan-4-yl)ethanone Chemical compound ClC(Cl)C(=O)N1CCOC11CCCCC1 QWWHRELOCZEQNZ-UHFFFAOYSA-N 0.000 abstract 2
- ZAWPDPLWGKAAHU-UHFFFAOYSA-N 2,2-dichloro-n-[2-oxo-2-(prop-2-enylamino)ethyl]-n-prop-2-enylacetamide Chemical compound ClC(Cl)C(=O)N(CC=C)CC(=O)NCC=C ZAWPDPLWGKAAHU-UHFFFAOYSA-N 0.000 abstract 2
- OHXLAOJLJWLEIP-UHFFFAOYSA-N 2-(dichloromethyl)-2-methyl-1,3-dioxolane Chemical compound ClC(Cl)C1(C)OCCO1 OHXLAOJLJWLEIP-UHFFFAOYSA-N 0.000 abstract 2
- XULSMJYYEGLOOX-UHFFFAOYSA-N 4-(7-chloro-2,4-dimethyl-1-benzofuran-5-yl)-2-methyl-5-(trifluoromethyl)-1,2,4-triazole-3-thione Chemical compound C=1C(Cl)=C2OC(C)=CC2=C(C)C=1N1C(C(F)(F)F)=NN(C)C1=S XULSMJYYEGLOOX-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-UHFFFAOYSA-N 0.000 abstract 2
- LLQPHQFNMLZJMP-UHFFFAOYSA-N Fentrazamide Chemical compound N1=NN(C=2C(=CC=CC=2)Cl)C(=O)N1C(=O)N(CC)C1CCCCC1 LLQPHQFNMLZJMP-UHFFFAOYSA-N 0.000 abstract 2
- 239000005574 MCPA Substances 0.000 abstract 2
- VGHPMIFEKOFHHQ-UHFFFAOYSA-N Metosulam Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1S(=O)(=O)NC1=C(Cl)C=CC(C)=C1Cl VGHPMIFEKOFHHQ-UHFFFAOYSA-N 0.000 abstract 2
- RRKHIAYNPVQKEF-UHFFFAOYSA-N Pyriftalid Chemical compound COC1=CC(OC)=NC(SC=2C=3C(=O)OC(C)C=3C=CC=2)=N1 RRKHIAYNPVQKEF-UHFFFAOYSA-N 0.000 abstract 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 2
- 244000038559 crop plants Species 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical compound CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 abstract 2
- MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical compound C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 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
- FRJYTNTXOQQKRG-UHFFFAOYSA-N 1-(3-chloro-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridin-2-yl)-5-[methyl(propan-2-yl)amino]pyrazole-4-carbonitrile Chemical compound ClC=1C(=NN2C1CCCC2)N2N=CC(=C2N(C(C)C)C)C#N FRJYTNTXOQQKRG-UHFFFAOYSA-N 0.000 abstract 1
- 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 abstract 1
- OISQRMLHYOLTJL-UHFFFAOYSA-N 2,2-dichloro-n-(1,3-dioxolan-2-ylmethyl)-n-prop-2-enylacetamide Chemical compound ClC(Cl)C(=O)N(CC=C)CC1OCCO1 OISQRMLHYOLTJL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 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
- OGZUWSFEZCBGPH-UHFFFAOYSA-N 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylic acid Chemical compound OC(=O)C=1SC(Cl)=NC=1C(F)(F)F OGZUWSFEZCBGPH-UHFFFAOYSA-N 0.000 abstract 1
- QQSHXEQBULUEBP-UHFFFAOYSA-N 2-methoxy-n-[4-[(2-methoxyacetyl)amino]phenyl]sulfonylbenzamide Chemical compound C1=CC(NC(=O)COC)=CC=C1S(=O)(=O)NC(=O)C1=CC=CC=C1OC QQSHXEQBULUEBP-UHFFFAOYSA-N 0.000 abstract 1
- CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005711 Benzoic acid Substances 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- FCODLBLEKSFOLV-UHFFFAOYSA-N CN1N=CC(C(=O)C=2C(=C(C=3CCON=3)C(=CC=2)S(C)(=O)=O)Cl)=C1O Chemical compound CN1N=CC(C(=O)C=2C(=C(C=3CCON=3)C(=CC=2)S(C)(=O)=O)Cl)=C1O FCODLBLEKSFOLV-UHFFFAOYSA-N 0.000 abstract 1
- 239000005492 Carfentrazone-ethyl Substances 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
- 241000196324 Embryophyta Species 0.000 abstract 1
- GMBRUAIJEFRHFQ-UHFFFAOYSA-N Fenchlorazole-ethyl Chemical group N1=C(C(=O)OCC)N=C(C(Cl)(Cl)Cl)N1C1=CC=C(Cl)C=C1Cl GMBRUAIJEFRHFQ-UHFFFAOYSA-N 0.000 abstract 1
- UKSLKNUCVPZQCQ-UHFFFAOYSA-N Fluxofenim Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)=NOCC1OCCO1 UKSLKNUCVPZQCQ-UHFFFAOYSA-N 0.000 abstract 1
- LXKOADMMGWXPJQ-UHFFFAOYSA-N Halosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N(N=C(Cl)C=2C(O)=O)C)=N1 LXKOADMMGWXPJQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005582 Metosulam Substances 0.000 abstract 1
- IHHMUBRVTJMLQO-UHFFFAOYSA-N Pyraclonil Chemical compound C#CCN(C)C1=C(C#N)C=NN1C1=NN(CCCC2)C2=C1Cl IHHMUBRVTJMLQO-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 1
- WEVYAHXRMPXWCK-UHFFFAOYSA-N acetonitrile Substances CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- MKQSWTQPLLCSOB-UHFFFAOYSA-N benzyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound N1=C(Cl)SC(C(=O)OCC=2C=CC=CC=2)=C1C(F)(F)F MKQSWTQPLLCSOB-UHFFFAOYSA-N 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- FUHMZYWBSHTEDZ-UHFFFAOYSA-M bispyribac-sodium Chemical compound [Na+].COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C([O-])=O)=N1 FUHMZYWBSHTEDZ-UHFFFAOYSA-M 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- ICJSJAJWTWPSBD-UHFFFAOYSA-N cloquintocet Chemical compound C1=CN=C2C(OCC(=O)O)=CC=C(Cl)C2=C1 ICJSJAJWTWPSBD-UHFFFAOYSA-N 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- MLKCGVHIFJBRCD-UHFFFAOYSA-N ethyl 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoate Chemical group C1=C(Cl)C(CC(Cl)C(=O)OCC)=CC(N2C(N(C(F)F)C(C)=N2)=O)=C1F MLKCGVHIFJBRCD-UHFFFAOYSA-N 0.000 abstract 1
- 125000004494 ethyl ester group Chemical group 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- JCHMGYRXQDASJE-UHFFFAOYSA-N metcamifen Chemical compound C1=CC(NC(=O)NC)=CC=C1S(=O)(=O)NC(=O)C1=CC=CC=C1OC JCHMGYRXQDASJE-UHFFFAOYSA-N 0.000 abstract 1
- HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- PZQSQRCNMZGWFT-QXMHVHEDSA-N propan-2-yl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC(C)C PZQSQRCNMZGWFT-QXMHVHEDSA-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
- 230000001681 protective effect Effects 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 230000002195 synergetic effect Effects 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 210000001541 thymus gland Anatomy 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
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 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
- A01N43/713—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with four or more nitrogen atoms as the only ring hetero atoms
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
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
Se refiere a nuevas combinaciones de compuestos activos sinérgicas, herbicidas, que contienen, por un lado, un derivado de tetrazolinona conocido, y por otro lado, compuestos con actividad herbicida, conocidos y/o protectores y que pueden emplearse, con éxito especialmente bueno, para la lucha selectiva contra malas hierbas en diversos cultivos de plantas útiles. Reivindicación 1: Agentes, caracterizados por un contenido activo en una combinación de productos activos que abarca (a) el compuesto constituido por la 4-(2-clorofenil)-N-ciclohexil-N-etil-4,5-dihidro-5-oxo-1H-tetrazol-1-carboxamida (Fentrazamide) de la fórmula general (1) ("producto activo 1") y (b) uno o varios compuestos pertenecientes a un segundo grupo de herbicidas, que contiene los productos activos citados a continuación: ácido 2,6-bis[(4,6-dimetoxi-2-pirimidinil)oxi]-bezoico o sus sales, por ejemplo las sal de sodio (Bispyribac-sodico, conocido por la EP-A 321 846), difenil-metanona O-[2,6-bis[(4,6-dimetoxi-2-pirimidinil)oxi]benzoil]oxima (Pyribenzoxim, conocido por la EP-A 658 549), 7-[(4,6-dimetoxi-2-pirimidinil)tio]-3-metil-1(3H)-isobenzofuranona (Pyriftalid, conocido por la WO 91/05781), 1-(3-cloro-4,5,6,7-tetrahidropirazolo[1,5-a]piridin-2-il)-5-(metil-2-propinilamino)-1H-pirazol-4-carbonitrilo (Pyraclonil, conocido por la WO 94/08999), N-(2,6-dicloro-3-metilfenil)-5,7-dimetoxi-[1,2,4]triazolo[1,5-a]pirimidin-2-sulfonamida (Metosulam), ácido 2-[[[[(4-metoxi-6-metil-1,3,5-triazin-2-il)amino]-carbonil]-amino]-sulfonil]-benzoico (Metsulfuron), 3-cloro-5-[[[[(4,6-dimetoxi-2-pirimidinil)-amino]carbonil]-amino]-sulfonil]-1-metil-1H-pirazol-4-carboxilato de metilo (Halossulfuron), ésteres del ácido a-2-dicloro-5-[4-(diflúormetil)-4,5-dihidro-3-metil-5-oxo-1H-1,2,4-triazol-1-il]-4-flúor-bencenopropanóico, especialmente el éster de etilo (Carfentrazone-etilo), 4-[2-cloro-3-(4,5-dihidroisoxazol-3-il)-4-metilsulfonil-benzoil]-5-hidroxi-1-metil-1H-pirazol (conocido por la WO 98/31681), ácido 5-[4-bromo-1-metil-5-(triflúormetil)-1H-pirazol-3-il]-2-cloro-4-flúor-benzoico (éster de 1-metiletilo) (Fluazolate, conocido por la WO 92/06962), 2-[1-[[2-(4-clorofenoxi)-propoxi]amino]butil]-5-(tetrahidro-2H-tiopiran-3-il)-1,3-ciclohexadiona (Clefoxydim, conocido por la EP 456112), N-(2,4-diflúorfenil-1,5-dihidro-N-i-propil-5-oxo-1-[(tetrahidro-2H-piran-2-il)-metil]-4H-1,2,4-triazol-4-carboxamida (HOK-201 - véanse las publicaciones WO-A-98/38176 / US-A-6077814), 4-(7-cloro-2,4-dimetil-5-benzofuranil)-2,4-dihidro-2-metil-5-triflúormetil-3H-1,2,4-triazol-3-tiona (OK-701 - véanse las publicaciones WO-A-97/09326 / US-A-5759958), [2-cloro-3-(4,5-dihidro-3-isoxazolil)-4-metilsulfonil-fenil]-(5-hidroxi-1-metil-1H-pirazol-4-il)-metanona (véase las publicaciones WO-A-96/26206, WO-A-98/31681), [3-(4,5-dihidro-3-isoxazolil)-2-metil-4-metilsulfonil-fenil]-(5-hidroxi-1-metil-1H-pirazol-4-il)metanona (véase las publicaciones WO-A-96/26206, WO-A-98/31681), [3-[2-cloro-3(2,6-dioxo-ciclohexil)carbonil]-6-etilsulfonil-fenil]-5-isoxazolil]-acetonitrilo (véase la publicación WO-A-01/28341), 2-[2-cloro-4-metilsulfonil-3-[(2,2,2-triflúor-etoxi)-metil[-benzoil]-1,3-ciclohexano-diona (véase la publicación WO-A-01/28341) y 2-[[5,8-dimetil-1,1-dióxido-4-(2-pirimidiniloxi)-3,4-dihidro-2H-tiocromen-6-il]-carbonil]-1,3-ciclohexandiona (véase la piblicación WO-A-01/28341); (''productos activos del grupo 2''), así como, en caso dado c) al menos un compuesto mejorador de la compatibilidad para con las plantas de cultivo perteneciente al grupo siguiente de compuestos: a-(1,3-dioxolan-2-il-metoxiimino)-fenilacetonitrilo (Oxabetrinil), a-(ciano-metoxiimino)-fenilacetonitrilo (Cyometrinil), 4-cloro-N-(1,3-dioxolan-2-il-metoxi)-a-triflúor-acetofenonoxima (Fluxofenim), 4,6-dicloro-2-fenil-pirimidina (Fenclorim), 4-dicloroacetil-3,4-dihidro-3-metil-2H-1,4-benz-oxazina (Benoxacor), ácido 5-cloro-quinoxalin-8-oxi-acético (éster de 1-metil-hexilo) (Cloquintocet), 2,2-dicloro-N-(2-oxo-2-(2-propenilamino)-etil)-N-(2-propenil)-acetamida (DKA-24), anhídrido del ácido 1,8-naftálico, 1-(2,4-dicloro-fenil)-5-triclorometil-1H-1,2,4-triazol-3-carboxilato de etilo (Fenchlorazole-etilo), 2-cloro-4-triflúormetil-tiazol-5-carboxilato de fenilmetilo (Flurazole), 3-dicloroacetil-5-(2-furanil)-2,2-dimetil-oxazolidina (furilazole, MON-13900), 4-dicloroacetil-1-oxa-4-aza-spiro[4,5]-decano (AD-67), 2-dicloro-metil-2-metil-1,3-dioxolano (MG-191), 2,2-dicloro-N-(1,3-dioxolan-2-il-metil)-N-(2-propenil)-acetamida (PPG-1292), 2,2-dicloro-N-N-di-2-propenil-acetamida (Di-chlormid); N-(4-metil-fenil)-N'-(1-metil-1-fenil-etil)urea (Dymron), 1-di-cloroacetil-hexahidro-3,3,8a-trimetilpirrolo[1,2-a]-pirimidin-6(2H)-ona (BAS-145138), N-(2-metoxi-benzoil)-4-(metilaminocarbonilamino)-bencenosulfonamida, etil-4,5-dihidro-5,5-difenil-3-isoxazolcarboxilato (Isoxadifen-etilo), ácido (4-cloro-2-metilfenoxi)- acético (MCPA), ácido 2-(4-cloro-2-metildenoxi)-acético (MCPA), ácido 2-(4-cloro-2-metildenoxi)-propiónico 8Mercoprop), dietil-1-(2,4-dicloro-fenil)-4,5-dihidro-5-metil-1H-pirazol-3,5-dicarboxilato (Mefenpyr-dietilo), ácido 2,4-diclorofenoxiacético (2,4-D) y sus derivados, 4-(2-clorobenzoil-aminosulfonil)-N-propilbenzaqmida y otros derivados de N-(fenilsuilfamoil) bezamida de la fórmula (2) en al que R1 significa, hidrógeno, alquilo C1-6, cicloalquilo C3-6, alquenilo C2-6, cicloalquenilo C5-6, fenilo o heterociclilo con 3 a 6 miembros con hasta 3 heteroátomos del grupo formado por nitrógeno, oxígeno y azufre, estando sustituidos los seis restos, citado en último lugar, en caso dado, por uno o varios sustituyentes, iguales o diferentes, elegidos del grupo formado por halógeno, alcoxi C1-6, haloalcoxi C1-6, alquilsulfinilo C1-2, alquilsulfonilo C1-2, cicloalquilo C3-6, alcoxicarbonilo C1-4, alquilcarbonilo C1-4 y fenilo y, en el caso de los restos cíclicos, también alquilo C1-4 y haloalquilo C1-4; R2 significa hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, estando sustituidos los tres restos, citados en último lugar, en caso dado por uno o varios sustituyentes, iguales o diferentes, elegidos del grupo formado por halógeno, hidroxi, alquilo C1-4, alcoxi C1-4 y alquiltio C1-4; R3 significa haloalquilo C1-4, haloalcoxi C1-4, nitro, alquilo C1-4, alcoxi C1-4, alquilsulfonilo C1-4, alcoxicarbonilo C1-4, o alquilcarbonilo C1-4; R4 significa hidrógeno o metilo; R5 significa halógeno, nitro, alquilo C1-4, haloalquilo C1-4, haloalcoxi C1-4, cicloalquilo C3-6, fenilo, alcoxi C1-4, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, alcoxicarbonilo C1-4 o alquilcarbonilo C1-4; n significa 0, 1 ó 2 y m significa 1 ó 2 así como sus sales, especialmente las sales de sodio (Conocido por la WO- 099/16744) o la 2-metoxi-N-[4-(2-metoxibenzoilsulfamoil)fenil]-acetamida así como otros derivados de N-acilsulfonamida de la fórmula (3) en la que R1 significa hidrógeno, alquilo C1-6, cicloalquilo C3-6, furanilo o tienilo, estando cada uno de los cuatro restos citados en último lugar, insustituido o sustituido por uno o varios sustituyentes del grupo formado por halógeno, alcoxi C1-4, halógeno-alcoxi C1-6 y alquilo C1-4 y en el caso de los restos cíclicos, también alquilo C1-4 y halógenoalquilo C1-4; R2 significa hidrógeno o metilo; R3 significa halógeno, halógeno-alquilo C1-4, halógeno-alcoxi C1-4, alquilo C1-4, alcoxi C1-4, alquilsulfonilo C1-4, alcoxicarbonilo C1-4, alquilcarbonilo C1-4; R4 significa hidrógeno o metilo, R5 significa halógeno, alquilo C1-4, halógeno-alquilo C1-4, halógeno-alcoxi C1-4, cicloalquilo C3-6, fenilo, alcoxi C1-4, ciano, alquiltio C1-4, alquilsulfinilo C1-4, alquilsulfonilo C1-4, alcoxicarbonilo C1-4, alquilcarbonilo C1-4; n significa 0, 1 ó 2 y m significa 1 ó 2, así como sus sales con metales alcalinos, especialmente las sales de sodio (conocido por la DE-A1-19 621 522). (''Productos activos del grupo 3'').
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10142336A DE10142336A1 (de) | 2001-08-30 | 2001-08-30 | Selektive Herbizide enthaltend ein Tetrazolinon-Derivat |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR035286A1 true AR035286A1 (es) | 2004-05-05 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020103126A AR035286A1 (es) | 2001-08-30 | 2002-08-20 | Herbicidas selectivos que contienen un derivado de tetrazolinona. |
Country Status (15)
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| US (1) | US7202196B2 (es) |
| EP (1) | EP1423010A2 (es) |
| JP (1) | JP2005501876A (es) |
| KR (1) | KR20040029033A (es) |
| CN (1) | CN1277472C (es) |
| AR (1) | AR035286A1 (es) |
| BR (1) | BR0212255A (es) |
| CO (1) | CO5560518A2 (es) |
| DE (1) | DE10142336A1 (es) |
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| MY (1) | MY131067A (es) |
| PL (1) | PL368852A1 (es) |
| RU (1) | RU2004109590A (es) |
| TW (1) | TWI254611B (es) |
| WO (1) | WO2003020035A2 (es) |
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| ES2407657T3 (es) * | 2006-03-28 | 2013-06-13 | Riceco, Llc | Efectos sinérgicos de los herbicidas inhibidores de la ALS cuando se combinan con propanil |
| DE102007028019A1 (de) * | 2007-06-19 | 2008-12-24 | Bayer Cropscience Ag | Synergistische kulturpflanzenverträgliche Kombinationen enthaltend Herbizide aus der Gruppe der Benzoylcyclohexandione für den Einsatz in Reis-Kulturen |
| US20110092554A1 (en) * | 2007-11-19 | 2011-04-21 | Richard Chesworth | 1,3,5 tri-subtituted benzenes for treatment of alzheimer's disease and other disorders |
| RU2527177C2 (ru) | 2007-12-20 | 2014-08-27 | Энвиво Фармасьютикалз, Инк. | Четырехзамещенные бензолы |
| KR100987193B1 (ko) * | 2008-07-01 | 2010-10-11 | 주식회사 금오조경개발 | 이동식 황토 찜질방 |
| CN102461555B (zh) * | 2010-11-19 | 2014-03-05 | 南京华洲药业有限公司 | 一种含醚磺隆、氰氟草酯与禾草敌的混合除草剂及其应用 |
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-
2001
- 2001-08-30 DE DE10142336A patent/DE10142336A1/de not_active Withdrawn
-
2002
- 2002-08-19 EP EP02792557A patent/EP1423010A2/de not_active Withdrawn
- 2002-08-19 BR BR0212255-3A patent/BR0212255A/pt not_active Application Discontinuation
- 2002-08-19 PL PL02368852A patent/PL368852A1/xx not_active Application Discontinuation
- 2002-08-19 JP JP2003524358A patent/JP2005501876A/ja active Pending
- 2002-08-19 MX MXPA04001904A patent/MXPA04001904A/es unknown
- 2002-08-19 RU RU2004109590/04A patent/RU2004109590A/ru not_active Application Discontinuation
- 2002-08-19 US US10/487,798 patent/US7202196B2/en not_active Expired - Fee Related
- 2002-08-19 CN CNB028212118A patent/CN1277472C/zh not_active Expired - Fee Related
- 2002-08-19 WO PCT/EP2002/009238 patent/WO2003020035A2/de not_active Ceased
- 2002-08-19 KR KR10-2004-7002754A patent/KR20040029033A/ko not_active Ceased
- 2002-08-20 AR ARP020103126A patent/AR035286A1/es not_active Application Discontinuation
- 2002-08-28 MY MYPI20023197A patent/MY131067A/en unknown
- 2002-08-29 TW TW091119613A patent/TWI254611B/zh not_active IP Right Cessation
-
2004
- 2004-03-18 CO CO04025942A patent/CO5560518A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| RU2004109590A (ru) | 2005-10-20 |
| US7202196B2 (en) | 2007-04-10 |
| KR20040029033A (ko) | 2004-04-03 |
| MY131067A (en) | 2007-07-31 |
| TWI254611B (en) | 2006-05-11 |
| MXPA04001904A (es) | 2004-06-15 |
| CN1575128A (zh) | 2005-02-02 |
| WO2003020035A3 (de) | 2003-09-04 |
| PL368852A1 (en) | 2005-04-04 |
| EP1423010A2 (de) | 2004-06-02 |
| JP2005501876A (ja) | 2005-01-20 |
| WO2003020035A2 (de) | 2003-03-13 |
| DE10142336A1 (de) | 2003-03-20 |
| US20050085388A1 (en) | 2005-04-21 |
| BR0212255A (pt) | 2004-10-19 |
| CO5560518A2 (es) | 2005-09-30 |
| CN1277472C (zh) | 2006-10-04 |
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