RU2004109590A - Селективные гербициды, содержащие производное тетразолинона - Google Patents
Селективные гербициды, содержащие производное тетразолинона Download PDFInfo
- Publication number
- RU2004109590A RU2004109590A RU2004109590/04A RU2004109590A RU2004109590A RU 2004109590 A RU2004109590 A RU 2004109590A RU 2004109590/04 A RU2004109590/04 A RU 2004109590/04A RU 2004109590 A RU2004109590 A RU 2004109590A RU 2004109590 A RU2004109590 A RU 2004109590A
- Authority
- RU
- Russia
- Prior art keywords
- carbon atoms
- methyl
- alkyl
- chloro
- group
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title claims 2
- JXBKZAYVMSNKHA-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-olate Chemical class OC=1N=NNN=1 JXBKZAYVMSNKHA-UHFFFAOYSA-N 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 59
- 125000000217 alkyl group Chemical group 0.000 claims 16
- 239000013543 active substance Substances 0.000 claims 12
- 125000003545 alkoxy group Chemical group 0.000 claims 12
- 229910052736 halogen Inorganic materials 0.000 claims 7
- 150000002367 halogens Chemical class 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- -1 2 , 4-difluorophenyl-1,5-dihydro-N-iso-propyl-5-oxo-1 - [(tetrahydro-2H-pyran-2-yl) methyl] -4H-1,2,4-triazole-4 -carboxamide Chemical compound 0.000 claims 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 4
- 125000004414 alkyl thio group Chemical group 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 125000004438 haloalkoxy group Chemical group 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 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 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 3
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 3
- 125000001188 haloalkyl group Chemical group 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 229910052708 sodium Inorganic materials 0.000 claims 3
- 239000011734 sodium Substances 0.000 claims 3
- 159000000000 sodium salts Chemical class 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 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 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 claims 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 2
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims 2
- 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 claims 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 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 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 2
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-UHFFFAOYSA-N 0.000 claims 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 claims 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 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 2
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 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 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 230000008635 plant growth Effects 0.000 claims 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 claims 1
- 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 claims 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 claims 1
- HXKWSTRRCHTUEC-UHFFFAOYSA-N 2,4-Dichlorophenoxyaceticacid Chemical compound OC(=O)C(Cl)OC1=CC=C(Cl)C=C1 HXKWSTRRCHTUEC-UHFFFAOYSA-N 0.000 claims 1
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 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 claims 1
- ARLANDKAVOHQOM-UHFFFAOYSA-N 2-(5,8-dimethyl-1,1-dioxo-4-pyrimidin-2-yloxy-3,4-dihydro-2h-thiochromene-6-carbonyl)cyclohexane-1,3-dione Chemical compound CC=1C=2C(OC=3N=CC=CN=3)CCS(=O)(=O)C=2C(C)=CC=1C(=O)C1C(=O)CCCC1=O ARLANDKAVOHQOM-UHFFFAOYSA-N 0.000 claims 1
- OHXLAOJLJWLEIP-UHFFFAOYSA-N 2-(dichloromethyl)-2-methyl-1,3-dioxolane Chemical compound ClC(Cl)C1(C)OCCO1 OHXLAOJLJWLEIP-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- GGYWEHUIXHXMJY-UHFFFAOYSA-N 2-[3-[2-chloro-3-(2,6-dioxocyclohexanecarbonyl)-6-ethylsulfonylphenyl]-1,2-oxazol-5-yl]acetonitrile Chemical compound ClC1=C(C2=NOC(CC#N)=C2)C(S(=O)(=O)CC)=CC=C1C(=O)C1C(=O)CCCC1=O GGYWEHUIXHXMJY-UHFFFAOYSA-N 0.000 claims 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 claims 1
- CAVRKMFXYXBJMA-UHFFFAOYSA-N 2-chloro-n-[4-(propylcarbamoyl)phenyl]sulfonylbenzamide Chemical compound C1=CC(C(=O)NCCC)=CC=C1S(=O)(=O)NC(=O)C1=CC=CC=C1Cl CAVRKMFXYXBJMA-UHFFFAOYSA-N 0.000 claims 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 claims 1
- YNMHKERYELPEEF-UHFFFAOYSA-N 4-bromo-3-(5'-carboxy-4'-chloro-2'-fluorophenyl)-1-methyl-5-trifluoromethyl-pyrazol Chemical compound BrC1=C(C(F)(F)F)N(C)N=C1C1=CC(C(O)=O)=C(Cl)C=C1F YNMHKERYELPEEF-UHFFFAOYSA-N 0.000 claims 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 claims 1
- PYKLUAIDKVVEOS-UHFFFAOYSA-N Cyometrinil Chemical compound N#CCON=C(C#N)C1=CC=CC=C1 PYKLUAIDKVVEOS-UHFFFAOYSA-N 0.000 claims 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 claims 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 claims 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 claims 1
- FMGZEUWROYGLAY-UHFFFAOYSA-N Halosulfuron-methyl Chemical compound ClC1=NN(C)C(S(=O)(=O)NC(=O)NC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OC FMGZEUWROYGLAY-UHFFFAOYSA-N 0.000 claims 1
- 239000005574 MCPA Substances 0.000 claims 1
- 239000005582 Metosulam Substances 0.000 claims 1
- 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 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 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 claims 1
- 229940088623 biologically active substance Drugs 0.000 claims 1
- 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 1
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 1
- 239000000945 filler Substances 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 229960004275 glycolic acid Drugs 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 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 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 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 1
- 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 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 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 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 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 claims 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 |
|---|---|---|---|
| DE10142336.5 | 2001-08-30 | ||
| DE10142336A DE10142336A1 (de) | 2001-08-30 | 2001-08-30 | Selektive Herbizide enthaltend ein Tetrazolinon-Derivat |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2004109590A true RU2004109590A (ru) | 2005-10-20 |
Family
ID=7697000
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2004109590/04A RU2004109590A (ru) | 2001-08-30 | 2002-08-19 | Селективные гербициды, содержащие производное тетразолинона |
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 |
|---|---|---|---|---|
| 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 |
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 |
| 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 |
| 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 |
| 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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-
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 |
|---|---|---|---|---|
| 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 |
Also Published As
| Publication number | Publication date |
|---|---|
| BR0212255A (pt) | 2004-10-19 |
| WO2003020035A2 (de) | 2003-03-13 |
| MXPA04001904A (es) | 2004-06-15 |
| JP2005501876A (ja) | 2005-01-20 |
| 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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