JP2005501876A5 - - Google Patents
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- JP2005501876A5 JP2005501876A5 JP2003524358A JP2003524358A JP2005501876A5 JP 2005501876 A5 JP2005501876 A5 JP 2005501876A5 JP 2003524358 A JP2003524358 A JP 2003524358A JP 2003524358 A JP2003524358 A JP 2003524358A JP 2005501876 A5 JP2005501876 A5 JP 2005501876A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- chloro
- alkyl
- dihydro
- alkoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- -1 EP 321846) Chemical compound 0.000 claims 12
- 150000001875 compounds Chemical class 0.000 claims 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 7
- 229910052736 halogen Inorganic materials 0.000 claims 7
- 150000002367 halogens Chemical class 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 3
- 159000000000 sodium salts Chemical class 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 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 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
- 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 2
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims 2
- 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 2
- OHXLAOJLJWLEIP-UHFFFAOYSA-N 2-(dichloromethyl)-2-methyl-1,3-dioxolane Chemical compound ClC(Cl)C1(C)OCCO1 OHXLAOJLJWLEIP-UHFFFAOYSA-N 0.000 claims 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 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 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
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
- 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
- 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 1
- 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 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
- 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
- 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 1
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 claims 1
- 239000005711 Benzoic acid Substances 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 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
- 229940126062 Compound A Drugs 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
- YRMLFORXOOIJDR-UHFFFAOYSA-N Dichlormid Chemical compound ClC(Cl)C(=O)N(CC=C)CC=C YRMLFORXOOIJDR-UHFFFAOYSA-N 0.000 claims 1
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-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
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 1
- 239000005574 MCPA Substances 0.000 claims 1
- 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 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 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 group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 235000010233 benzoic acid Nutrition 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
- 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
- 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 1
- 239000004067 bulking agent Substances 0.000 claims 1
- 229940047583 cetamide Drugs 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 244000038559 crop plants Species 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 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 1
- 125000004494 ethyl ester group Chemical group 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 claims 1
- 238000000034 method Methods 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
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 239000001301 oxygen Chemical group 0.000 claims 1
- 229910052760 oxygen Inorganic materials 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 Chemical group 0.000 claims 1
- 229910052717 sulfur Chemical group 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 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 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
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 0 CC(C(*)(CCC1)CCC1C(N(*)S(C(CCC1*)CCC1C(N(*)*)=O)(=O)=O)=O)S Chemical compound CC(C(*)(CCC1)CCC1C(N(*)S(C(CCC1*)CCC1C(N(*)*)=O)(=O)=O)=O)S 0.000 description 2
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 JP2005501876A (ja) | 2005-01-20 |
| JP2005501876A5 true JP2005501876A5 (https=) | 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 (https=) |
| EP (1) | EP1423010A2 (https=) |
| JP (1) | JP2005501876A (https=) |
| KR (1) | KR20040029033A (https=) |
| CN (1) | CN1277472C (https=) |
| AR (1) | AR035286A1 (https=) |
| BR (1) | BR0212255A (https=) |
| CO (1) | CO5560518A2 (https=) |
| DE (1) | DE10142336A1 (https=) |
| MX (1) | MXPA04001904A (https=) |
| MY (1) | MY131067A (https=) |
| PL (1) | PL368852A1 (https=) |
| RU (1) | RU2004109590A (https=) |
| TW (1) | TWI254611B (https=) |
| WO (1) | WO2003020035A2 (https=) |
Families Citing this family (16)
| 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 |
| WO2007112400A2 (en) * | 2006-03-28 | 2007-10-04 | 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 |
| WO2009067493A2 (en) * | 2007-11-19 | 2009-05-28 | Envivo Pharmaceuticals, Inc. | 1,3,5 tri-subtituted benzenes for treatment of alzheimer's disease and other disorders |
| JP2011507909A (ja) | 2007-12-20 | 2011-03-10 | エンビボ ファーマシューティカルズ インコーポレイテッド | 四置換ベンゼン |
| 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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| 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 |
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| 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 |
| DE59814338D1 (de) | 1997-01-17 | 2009-03-12 | Basf Se | 3-heteroxyclyl-substituierte benzoylderivate |
| AU6207698A (en) | 1997-01-17 | 1998-08-07 | Basf Aktiengesellschaft | Process for preparing sulphurous 2-chloro-3-(4,5-dihydroisoxazol-3-yl)-benzoic acids |
| 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 |
| US6077814A (en) | 1997-02-26 | 2000-06-20 | 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 |
| EP1104232B8 (de) | 1998-07-16 | 2010-10-27 | Bayer CropScience AG | Herbizide mittel |
| 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 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 KR KR10-2004-7002754A patent/KR20040029033A/ko not_active Ceased
- 2002-08-19 JP JP2003524358A patent/JP2005501876A/ja active Pending
- 2002-08-19 BR BR0212255-3A patent/BR0212255A/pt not_active Application Discontinuation
- 2002-08-19 CN CNB028212118A patent/CN1277472C/zh not_active Expired - Fee Related
- 2002-08-19 EP EP02792557A patent/EP1423010A2/de not_active Withdrawn
- 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 WO PCT/EP2002/009238 patent/WO2003020035A2/de 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
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