JP2005501876A - テトラゾリノン誘導体を含む選択的除草剤 - Google Patents
テトラゾリノン誘導体を含む選択的除草剤 Download PDFInfo
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- JP2005501876A JP2005501876A JP2003524358A JP2003524358A JP2005501876A JP 2005501876 A JP2005501876 A JP 2005501876A JP 2003524358 A JP2003524358 A JP 2003524358A JP 2003524358 A JP2003524358 A JP 2003524358A JP 2005501876 A JP2005501876 A JP 2005501876A
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- methyl
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- 239000004009 herbicide Substances 0.000 title claims abstract description 18
- JXBKZAYVMSNKHA-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-olate Chemical class OC=1N=NNN=1 JXBKZAYVMSNKHA-UHFFFAOYSA-N 0.000 title abstract description 7
- 150000001875 compounds Chemical class 0.000 claims abstract description 96
- 239000000203 mixture Substances 0.000 claims abstract description 61
- 238000009472 formulation Methods 0.000 claims abstract description 42
- -1 EP 321846) Chemical compound 0.000 claims description 66
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 16
- 244000038559 crop plants Species 0.000 claims description 15
- 229910052736 halogen Inorganic materials 0.000 claims description 14
- 150000002367 halogens Chemical class 0.000 claims description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- 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 claims description 8
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 8
- 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 claims description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 6
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 159000000000 sodium salts Chemical class 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 5
- NNYRZQHKCHEXSD-UHFFFAOYSA-N Daimuron Chemical compound C1=CC(C)=CC=C1NC(=O)NC(C)(C)C1=CC=CC=C1 NNYRZQHKCHEXSD-UHFFFAOYSA-N 0.000 claims description 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 5
- 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 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 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 claims description 4
- 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 claims description 4
- 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 claims description 4
- OHXLAOJLJWLEIP-UHFFFAOYSA-N 2-(dichloromethyl)-2-methyl-1,3-dioxolane Chemical compound ClC(Cl)C1(C)OCCO1 OHXLAOJLJWLEIP-UHFFFAOYSA-N 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- HXKWSTRRCHTUEC-UHFFFAOYSA-N 2,4-Dichlorophenoxyaceticacid Chemical compound OC(=O)C(Cl)OC1=CC=C(Cl)C=C1 HXKWSTRRCHTUEC-UHFFFAOYSA-N 0.000 claims description 3
- 239000005574 MCPA Substances 0.000 claims description 3
- 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 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 125000004494 ethyl ester group Chemical group 0.000 claims description 3
- 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 claims description 3
- 229910052717 sulfur Chemical group 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- 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 claims description 2
- HKELWJONQIFBPO-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1,2,4-triazole-3-carboxylic acid Chemical compound N1=C(C(=O)O)N=C(C(Cl)(Cl)Cl)N1C1=CC=C(Cl)C=C1Cl HKELWJONQIFBPO-UHFFFAOYSA-N 0.000 claims description 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 claims description 2
- UCULCNDQARIDMX-UHFFFAOYSA-N 2-[1-[2-(4-chlorophenoxy)propoxyamino]butyl]-5-(thian-3-yl)cyclohexane-1,3-dione Chemical compound O=C1CC(C2CSCCC2)CC(=O)C1C(CCC)NOCC(C)OC1=CC=C(Cl)C=C1 UCULCNDQARIDMX-UHFFFAOYSA-N 0.000 claims description 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 claims description 2
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 claims description 2
- 239000005711 Benzoic acid Substances 0.000 claims description 2
- 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 claims description 2
- PYKLUAIDKVVEOS-UHFFFAOYSA-N Cyometrinil Chemical compound N#CCON=C(C#N)C1=CC=CC=C1 PYKLUAIDKVVEOS-UHFFFAOYSA-N 0.000 claims description 2
- YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 claims description 2
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 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 claims description 2
- IHHMUBRVTJMLQO-UHFFFAOYSA-N Pyraclonil Chemical compound C#CCN(C)C1=C(C#N)C=NN1C1=NN(CCCC2)C2=C1Cl IHHMUBRVTJMLQO-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 235000010233 benzoic acid Nutrition 0.000 claims description 2
- 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 claims description 2
- RYVIXQCRCQLFCM-UHFFFAOYSA-N bispyribac Chemical compound COC1=CC(OC)=NC(OC=2C(=C(OC=3N=C(OC)C=C(OC)N=3)C=CC=2)C(O)=O)=N1 RYVIXQCRCQLFCM-UHFFFAOYSA-N 0.000 claims description 2
- 239000004067 bulking agent Substances 0.000 claims description 2
- 229940047583 cetamide Drugs 0.000 claims description 2
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 claims description 2
- WFVUIONFJOAYPK-UHFFFAOYSA-N n-(1,3-dioxolan-2-ylmethoxy)benzenecarboximidoyl cyanide Chemical compound C=1C=CC=CC=1C(C#N)=NOCC1OCCO1 WFVUIONFJOAYPK-UHFFFAOYSA-N 0.000 claims description 2
- BVFMYNNAEUPDCO-UHFFFAOYSA-N n-(phenylsulfamoyl)benzamide Chemical class C=1C=CC=CC=1C(=O)NS(=O)(=O)NC1=CC=CC=C1 BVFMYNNAEUPDCO-UHFFFAOYSA-N 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 239000001301 oxygen Chemical group 0.000 claims description 2
- 239000011593 sulfur Chemical group 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- IUQAXCIUEPFPSF-UHFFFAOYSA-N tembotrione Chemical compound ClC1=C(COCC(F)(F)F)C(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O IUQAXCIUEPFPSF-UHFFFAOYSA-N 0.000 claims description 2
- 125000001544 thienyl group Chemical group 0.000 claims description 2
- 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 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 7
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- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
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- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
- 229940126062 Compound A Drugs 0.000 claims 1
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
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- AWLUSOLTCFEHNE-UHFFFAOYSA-N sodium;urea Chemical compound [Na].NC(N)=O AWLUSOLTCFEHNE-UHFFFAOYSA-N 0.000 description 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 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- VLCQZHSMCYCDJL-UHFFFAOYSA-N tribenuron methyl Chemical compound COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 VLCQZHSMCYCDJL-UHFFFAOYSA-N 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 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 description 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 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- AXORVIZLPOGIRG-UHFFFAOYSA-N β-methylphenethylamine Chemical compound NCC(C)C1=CC=CC=C1 AXORVIZLPOGIRG-UHFFFAOYSA-N 0.000 description 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
- 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
-
- 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
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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10142336A DE10142336A1 (de) | 2001-08-30 | 2001-08-30 | Selektive Herbizide enthaltend ein Tetrazolinon-Derivat |
| PCT/EP2002/009238 WO2003020035A2 (de) | 2001-08-30 | 2002-08-19 | Selektive herbizide enthaltend ein tetrazolinon-derivat |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005501876A true JP2005501876A (ja) | 2005-01-20 |
| JP2005501876A5 JP2005501876A5 (enExample) | 2006-01-05 |
Family
ID=7697000
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003524358A Pending JP2005501876A (ja) | 2001-08-30 | 2002-08-19 | テトラゾリノン誘導体を含む選択的除草剤 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US7202196B2 (enExample) |
| EP (1) | EP1423010A2 (enExample) |
| JP (1) | JP2005501876A (enExample) |
| KR (1) | KR20040029033A (enExample) |
| CN (1) | CN1277472C (enExample) |
| AR (1) | AR035286A1 (enExample) |
| BR (1) | BR0212255A (enExample) |
| CO (1) | CO5560518A2 (enExample) |
| DE (1) | DE10142336A1 (enExample) |
| MX (1) | MXPA04001904A (enExample) |
| MY (1) | MY131067A (enExample) |
| PL (1) | PL368852A1 (enExample) |
| RU (1) | RU2004109590A (enExample) |
| TW (1) | TWI254611B (enExample) |
| WO (1) | WO2003020035A2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010530382A (ja) * | 2007-06-19 | 2010-09-09 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | 稲作に施用するためのベンゾイルシクロヘキサンジオン群からの相乗的作物耐性除草剤の組み合わせ |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102005031789A1 (de) * | 2005-07-07 | 2007-01-18 | Bayer Cropscience Gmbh | Kulturpflanzenverträgliche herbizide Mittel enthaltend Herbizide Safener |
| EP1998613B9 (en) * | 2006-03-28 | 2013-08-21 | Riceco, LLC | The synergistic effects of als inhibitor herbicides when combined with propanil |
| 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 |
| AU2008345573B2 (en) | 2007-12-20 | 2013-12-19 | Envivo Pharmaceuticals, Inc. | Tetrasubstituted benzenes |
| 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 |
| CN102461510A (zh) * | 2010-11-19 | 2012-05-23 | 南京华洲药业有限公司 | 一种含双草醚和克草胺的混合除草组合物 |
| RU2456800C1 (ru) * | 2011-05-05 | 2012-07-27 | Государственное бюджетное учреждение Республики Башкортостан "Научно-исследовательский технологический институт гербицидов и регуляторов роста растений с опытно-экспериментальным производством Академии наук Республики Башкортостан" | Гербицидная композиция |
| CN102228047A (zh) * | 2011-05-06 | 2011-11-02 | 浙江泰达作物科技有限公司 | 除草剂苯噻酰草胺与乙氧磺隆复配的水分散性粒剂及其制备方法 |
| CN102228026B (zh) * | 2011-05-25 | 2014-11-12 | 陕西韦尔奇作物保护有限公司 | 一种含双草醚与嘧啶氧(硫)苯甲酸酯类的除草组合物 |
| CN103039490B (zh) * | 2012-12-26 | 2015-01-21 | 山东滨农科技有限公司 | 一种含有四唑酰草胺和哒草特的除草组合物 |
| CN103636650A (zh) * | 2013-10-30 | 2014-03-19 | 广东中迅农科股份有限公司 | 一种含有四唑酰草胺和氯吡嘧磺隆的除草组合物 |
| CN104757013A (zh) * | 2015-04-18 | 2015-07-08 | 广东中迅农科股份有限公司 | 含有双唑草腈和四唑酰草胺及精噁唑禾草灵的除草组合物 |
| CN105052980A (zh) * | 2015-07-17 | 2015-11-18 | 安徽常泰化工有限公司 | 一种含四唑酰草胺的除草微乳剂 |
| CN106614600B (zh) * | 2016-06-26 | 2019-08-16 | 江苏中旗科技股份有限公司 | 一种针对水稻安全的除草组合物 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3853622T2 (de) * | 1987-12-22 | 1996-01-11 | Ihara Chemical Ind Co | Pyrimidin-Derivate, Verfahren zu deren Herstellung und herbizide Methode und Zusammenstellungen. |
| JP2813900B2 (ja) * | 1989-09-28 | 1998-10-22 | クミアイ化学工業株式会社 | 除草剤組成物 |
| EP0447506B1 (de) * | 1989-10-12 | 1994-10-26 | Ciba-Geigy Ag | Pyrimidin- und triazin-derivate mit herbizider und pflanzenwachstumsregulierender wirkung |
| DE59010569D1 (de) * | 1990-01-10 | 1996-12-19 | Hoechst Schering Agrevo Gmbh | Pyridylsulfonylharnstoffe als herbizide und pflanzenwachstumsregulatoren, verfahren zu ihrer herstellung und ihre verwendung |
| US5529976A (en) * | 1990-01-10 | 1996-06-25 | Hoechst Aktiengesellschaft | Pyridyl sulphonyl ureas as herbicides and plant growth regulators |
| EP0456112B1 (de) * | 1990-05-09 | 1994-08-31 | BASF Aktiengesellschaft | Cyclohexenonoximether, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide |
| US5600008A (en) * | 1990-10-18 | 1997-02-04 | Monsanto Company | Benzoyl derivatives and synthesis thereof |
| US5281571A (en) * | 1990-10-18 | 1994-01-25 | Monsanto Company | Herbicidal benzoxazinone- and benzothiazinone-substituted pyrazoles |
| US5532416A (en) * | 1994-07-20 | 1996-07-02 | Monsanto Company | Benzoyl derivatives and synthesis thereof |
| EP0663913B1 (en) * | 1992-10-12 | 1998-07-29 | Hoechst Schering AgrEvo GmbH | New substituted pyrazole derivatives, processes for their preparation and their use as herbicides |
| JP2822143B2 (ja) | 1993-02-25 | 1998-11-11 | 日本バイエルアグロケム株式会社 | テトラゾリノン類の水田用除草剤としての利用 |
| US5521146A (en) * | 1993-11-13 | 1996-05-28 | Lucky Ltd. | Herbicidal pyrimidine derivatives, process for preparation thereof and their use as herbicide |
| US6077813A (en) * | 1994-05-04 | 2000-06-20 | Bayer Aktiengesellschaft | Substituted aromatic thiocarboxylic acid amides and their use as herbicides |
| AU710172B2 (en) * | 1995-02-24 | 1999-09-16 | Basf Aktiengesellschaft | Pyrazolylbenzoyl derivatives |
| JP3772994B2 (ja) | 1995-06-22 | 2006-05-10 | バイエルクロップサイエンス株式会社 | 水田用農薬粒剤 |
| DE69605529T2 (de) * | 1995-09-07 | 2000-07-27 | Otsuka Kagaku K.K., Osaka | Thiazol-derivate, diese enthaltende herbizide und verfahren zu deren anwendung |
| JPH09241109A (ja) * | 1996-03-05 | 1997-09-16 | Nippon Bayeragrochem Kk | 除草剤組成物 |
| DE19621522A1 (de) * | 1996-05-29 | 1997-12-04 | Hoechst Schering Agrevo Gmbh | Neue N-Acylsulfonamide, neue Mischungen aus Herbiziden und Antidots und deren Verwendung |
| US6165944A (en) * | 1997-01-17 | 2000-12-26 | Basf Aktiengesellschaft | 4-(3-heterocyclyl-1-benzoyl) pyrazoles and their use as herbicides |
| DE59808163D1 (de) * | 1997-01-17 | 2003-06-05 | Basf Ag | Verfahren zur herstellung von schwefelhaltigen 2-chlor-3-(4,5-dihydroisoxazol-3-yl)-benzoesäuren |
| GEP20022617B (en) | 1997-01-17 | 2002-01-25 | Basf Ag | 3-Heterocyclic YL-Substituted Benzoyl Derivatives, Method for Their Production, Herbicidal Preparation and Method for Undesirable Plants Control |
| US5928991A (en) * | 1997-01-21 | 1999-07-27 | Bayer Aktiengesellschaft | Selective herbicides based on 1-(2-chloro-phenyl)-4-(N-cyclohexyl-N-ethyl-aminocarbonyl)-1,4-dihydro-5H-tetrazol-5-one and Propanil |
| WO1998038176A1 (en) * | 1997-02-26 | 1998-09-03 | Hokko Chemical Industry Co., Ltd. | 1-substituted 4-carbamoyl-1,2,4-triazol-5-one derivatives and herbicide |
| JP4065041B2 (ja) | 1997-05-30 | 2008-03-19 | バイエルクロップサイエンス株式会社 | 水性懸濁状除草剤組成物及び雑草防除方法 |
| AU744797B2 (en) | 1997-07-16 | 2002-03-07 | Syngenta Limited | Herbicidal compositions of tetrazolinone herbicides and antidotes therefor |
| DE19742951A1 (de) * | 1997-09-29 | 1999-04-15 | Hoechst Schering Agrevo Gmbh | Acylsulfamoylbenzoesäureamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung |
| JPH11335212A (ja) | 1998-05-21 | 1999-12-07 | Nippon Bayer Agrochem Co Ltd | 水田用除草剤組成物 |
| TR200100101T2 (tr) | 1998-07-16 | 2001-06-21 | Aventis Cropscience Gmbh | Herbisit ilaçlar. |
| DE19832017A1 (de) | 1998-07-16 | 2000-01-27 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel mit substituierten Phenylsulfonylharnstoffen zur Unkrautbekämpfung in Reis |
| JP2000239111A (ja) | 1999-02-19 | 2000-09-05 | Nippon Bayer Agrochem Co Ltd | 水田用除草剤混合組成物 |
| DE19947918A1 (de) * | 1999-10-06 | 2001-04-12 | Bayer Ag | Selektive Herbizide auf Basis von Pyrimidin-Derivaten |
| DE19950943A1 (de) | 1999-10-22 | 2001-05-17 | Aventis Cropscience Gmbh | Synergistische herbizide Mittel enthaltend Herbizide aus der Gruppe der Hemmstoffe der Hydroxyphenylpyruvat-Dioxygenase |
-
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 MX MXPA04001904A patent/MXPA04001904A/es unknown
- 2002-08-19 BR BR0212255-3A patent/BR0212255A/pt not_active Application Discontinuation
- 2002-08-19 KR KR10-2004-7002754A patent/KR20040029033A/ko not_active Ceased
- 2002-08-19 US US10/487,798 patent/US7202196B2/en not_active Expired - Fee Related
- 2002-08-19 PL PL02368852A patent/PL368852A1/xx not_active Application Discontinuation
- 2002-08-19 RU RU2004109590/04A patent/RU2004109590A/ru not_active Application Discontinuation
- 2002-08-19 WO PCT/EP2002/009238 patent/WO2003020035A2/de not_active Ceased
- 2002-08-19 CN CNB028212118A patent/CN1277472C/zh not_active Expired - Fee Related
- 2002-08-19 JP JP2003524358A patent/JP2005501876A/ja active Pending
- 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
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010530382A (ja) * | 2007-06-19 | 2010-09-09 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | 稲作に施用するためのベンゾイルシクロヘキサンジオン群からの相乗的作物耐性除草剤の組み合わせ |
Also Published As
| Publication number | Publication date |
|---|---|
| BR0212255A (pt) | 2004-10-19 |
| WO2003020035A2 (de) | 2003-03-13 |
| MXPA04001904A (es) | 2004-06-15 |
| RU2004109590A (ru) | 2005-10-20 |
| TWI254611B (en) | 2006-05-11 |
| CN1575128A (zh) | 2005-02-02 |
| EP1423010A2 (de) | 2004-06-02 |
| KR20040029033A (ko) | 2004-04-03 |
| AR035286A1 (es) | 2004-05-05 |
| WO2003020035A3 (de) | 2003-09-04 |
| DE10142336A1 (de) | 2003-03-20 |
| PL368852A1 (en) | 2005-04-04 |
| US7202196B2 (en) | 2007-04-10 |
| CN1277472C (zh) | 2006-10-04 |
| CO5560518A2 (es) | 2005-09-30 |
| US20050085388A1 (en) | 2005-04-21 |
| MY131067A (en) | 2007-07-31 |
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