JP2011520778A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2011520778A5 JP2011520778A5 JP2011500217A JP2011500217A JP2011520778A5 JP 2011520778 A5 JP2011520778 A5 JP 2011520778A5 JP 2011500217 A JP2011500217 A JP 2011500217A JP 2011500217 A JP2011500217 A JP 2011500217A JP 2011520778 A5 JP2011520778 A5 JP 2011520778A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- unsubstituted
- alkyl
- group
- amino
- 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.)
- Granted
Links
- 125000005843 halogen group Chemical group 0.000 claims description 136
- -1 formyloxy group Chemical group 0.000 claims description 60
- 150000001875 compounds Chemical class 0.000 claims description 33
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 29
- 125000003118 aryl group Chemical group 0.000 claims description 14
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 13
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 11
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 10
- 150000002923 oximes Chemical class 0.000 claims description 10
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 9
- 125000003277 amino group Chemical group 0.000 claims description 9
- 125000000623 heterocyclic group Chemical group 0.000 claims description 9
- 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 7
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 7
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 7
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 3
- 125000001188 haloalkyl group Chemical group 0.000 claims description 3
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 241001024304 Mino Species 0.000 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 claims description 2
- 239000002184 metal Chemical class 0.000 claims description 2
- 229910052752 metalloid Inorganic materials 0.000 claims description 2
- 150000002738 metalloids Chemical class 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 12
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 claims 4
- LKJPYSCBVHEWIU-UHFFFAOYSA-N N-[4-cyano-3-(trifluoromethyl)phenyl]-3-[(4-fluorophenyl)sulfonyl]-2-hydroxy-2-methylpropanamide Chemical compound C=1C=C(C#N)C(C(F)(F)F)=CC=1NC(=O)C(O)(C)CS(=O)(=O)C1=CC=C(F)C=C1 LKJPYSCBVHEWIU-UHFFFAOYSA-N 0.000 claims 4
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims 4
- 239000000758 substrate Substances 0.000 claims 4
- 239000002253 acid Substances 0.000 claims 3
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims 3
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 claims 3
- 125000005129 aryl carbonyl group Chemical group 0.000 claims 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 claims 2
- SHNUBALDGXWUJI-UHFFFAOYSA-N pyridin-2-ylmethanol Chemical compound OCC1=CC=CC=N1 SHNUBALDGXWUJI-UHFFFAOYSA-N 0.000 claims 2
- YSYILILRFKOSMG-UHFFFAOYSA-N 4-(chloromethyl)-n-methyl-1,3-thiazol-2-amine Chemical compound CNC1=NC(CCl)=CS1 YSYILILRFKOSMG-UHFFFAOYSA-N 0.000 claims 1
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 1
- 241000233866 Fungi Species 0.000 claims 1
- 241000607479 Yersinia pestis Species 0.000 claims 1
- 239000012872 agrochemical composition Substances 0.000 claims 1
- 125000005997 bromomethyl group Chemical group 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- LTVOKYUPTHZZQH-UHFFFAOYSA-N difluoromethane Chemical group F[C]F LTVOKYUPTHZZQH-UHFFFAOYSA-N 0.000 claims 1
- 235000013399 edible fruits Nutrition 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- LXFUIDQWOBQJOE-UHFFFAOYSA-N ethyl 6-[(2-methylpropan-2-yl)oxycarbonylamino]pyridine-2-carboxylate Chemical compound CCOC(=O)C1=CC=CC(NC(=O)OC(C)(C)C)=N1 LXFUIDQWOBQJOE-UHFFFAOYSA-N 0.000 claims 1
- 125000004494 ethyl ester group Chemical group 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 1
- 238000007654 immersion Methods 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- SSXZSQHXBWITRI-UHFFFAOYSA-N methyl 6-[(2-methylpropan-2-yl)oxycarbonylamino]pyridine-2-carboxylate Chemical compound COC(=O)C1=CC=CC(NC(=O)OC(C)(C)C)=N1 SSXZSQHXBWITRI-UHFFFAOYSA-N 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 1
- OZYPPHLDZUUCCI-UHFFFAOYSA-N n-(6-bromopyridin-2-yl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC1=CC=CC(Br)=N1 OZYPPHLDZUUCCI-UHFFFAOYSA-N 0.000 claims 1
- ZKDMTGFOPIELEE-UHFFFAOYSA-N n-(6-bromopyridin-2-yl)-2-methylpropanamide Chemical compound CC(C)C(=O)NC1=CC=CC(Br)=N1 ZKDMTGFOPIELEE-UHFFFAOYSA-N 0.000 claims 1
- AZKOTMZRXXAOOB-UHFFFAOYSA-N n-(6-bromopyridin-2-yl)acetamide Chemical compound CC(=O)NC1=CC=CC(Br)=N1 AZKOTMZRXXAOOB-UHFFFAOYSA-N 0.000 claims 1
- YPWKLBCTOUEZKE-UHFFFAOYSA-N n-(6-chloropyridin-2-yl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC1=CC=CC(Cl)=N1 YPWKLBCTOUEZKE-UHFFFAOYSA-N 0.000 claims 1
- DRJJATMNDDRQOM-UHFFFAOYSA-N n-(6-formylpyridin-2-yl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC1=CC=CC(C=O)=N1 DRJJATMNDDRQOM-UHFFFAOYSA-N 0.000 claims 1
- SSXGDEUEONGPAF-UHFFFAOYSA-N n-(6-formylpyridin-2-yl)acetamide Chemical compound CC(=O)NC1=CC=CC(C=O)=N1 SSXGDEUEONGPAF-UHFFFAOYSA-N 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- GHLZUHZBBNDWHW-UHFFFAOYSA-N nonanamide Chemical compound CCCCCCCCC(N)=O GHLZUHZBBNDWHW-UHFFFAOYSA-N 0.000 claims 1
- 231100001184 nonphytotoxic Toxicity 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- 230000003032 phytopathogenic effect Effects 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 239000008262 pumice Substances 0.000 claims 1
- 239000002994 raw material Substances 0.000 claims 1
- 239000002689 soil Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- BNLOFXUVYJUBJM-UHFFFAOYSA-N tert-butyl n-(6-formylpyridin-2-yl)carbamate Chemical compound CC(C)(C)OC(=O)NC1=CC=CC(C=O)=N1 BNLOFXUVYJUBJM-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 0 *[n]1nnnc1N Chemical compound *[n]1nnnc1N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 125000006727 (C1-C6) alkenyl group Chemical group 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08356047 | 2008-03-19 | ||
| EP08356047.4 | 2008-03-19 | ||
| PCT/EP2009/053208 WO2009115557A2 (en) | 2008-03-19 | 2009-03-18 | Fungicide hydroximoyl-tetrazole derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011520778A JP2011520778A (ja) | 2011-07-21 |
| JP2011520778A5 true JP2011520778A5 (enExample) | 2011-09-15 |
| JP5571062B2 JP5571062B2 (ja) | 2014-08-13 |
Family
ID=39673452
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011500217A Expired - Fee Related JP5571062B2 (ja) | 2008-03-19 | 2009-03-18 | 殺真菌剤ヒドロキシモイル−テトラゾール誘導体 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US8466176B2 (enExample) |
| EP (1) | EP2265118A2 (enExample) |
| JP (1) | JP5571062B2 (enExample) |
| KR (1) | KR20100125424A (enExample) |
| CN (1) | CN101977504B (enExample) |
| BR (1) | BRPI0906023A2 (enExample) |
| CO (1) | CO6280584A2 (enExample) |
| MX (1) | MX2010010135A (enExample) |
| WO (1) | WO2009115557A2 (enExample) |
| ZA (1) | ZA201006312B (enExample) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9060518B2 (en) * | 2008-01-15 | 2015-06-23 | Pierre-Yves Coqueron | Pesticide composition comprising a tetrazolyloxime derivative and a fungicide or an insecticide active substance |
| JP2011515368A (ja) * | 2008-03-19 | 2011-05-19 | 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 | 殺菌剤ヒドロキシモイル−テトラゾール誘導体 |
| CN101977502A (zh) * | 2008-03-19 | 2011-02-16 | 拜尔农科股份公司 | 杀真菌剂肟基-四唑衍生物 |
| EP2303865B1 (en) * | 2008-07-04 | 2014-06-11 | Bayer Intellectual Property GmbH | Fungicide hydroximoyl-tetrazole derivatives |
| BRPI0910178A8 (pt) * | 2008-07-04 | 2015-11-24 | Bayer Cropscience Ag | "composto de fórmula (i), composto de fórmula (vi), composição de fungicidas e método para o controle de fungo fitopatogênico de culturas" |
| JP5550913B2 (ja) * | 2009-01-05 | 2014-07-16 | 日本曹達株式会社 | テトラゾイルオキシム誘導体およびその塩、並びに植物病害防除剤 |
| JP5542452B2 (ja) * | 2009-01-05 | 2014-07-09 | 日本曹達株式会社 | テトラゾイルオキシム誘導体およびその塩、ならびに植物病害防除剤 |
| TW201138624A (en) * | 2009-12-28 | 2011-11-16 | Bayer Cropscience Ag | Fungicide hydroximoyl-tetrazole derivatives |
| JP5627038B2 (ja) * | 2010-03-12 | 2014-11-19 | 日本曹達株式会社 | ピリジン環含有化合物 |
| AU2014201038B2 (en) * | 2010-04-06 | 2015-08-06 | Nippon Soda Co., Ltd. | Nitrogen-containing heterocyclic compound and method for producing same |
| WO2011125568A1 (ja) * | 2010-04-06 | 2011-10-13 | 日本曹達株式会社 | 含窒素複素環化合物及びその製造方法 |
| WO2011134911A2 (en) * | 2010-04-28 | 2011-11-03 | Bayer Cropscience Ag | Fungicide hydroximoyl-tetrazole derivatives |
| JP5977242B2 (ja) * | 2010-10-07 | 2016-08-24 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | テトラゾリルオキシム誘導体とチアゾリルピペリジン誘導体を含んでいる殺菌剤組成物 |
| WO2012117021A2 (en) * | 2011-03-03 | 2012-09-07 | Syngenta Participations Ag | Novel microbiocidal oxime ethers |
| BR112014020610B8 (pt) * | 2012-03-13 | 2020-03-10 | Nippon Soda Co | composto, métodos para produzir e para purificar a forma (z) de um composto, e para produzir a forma (z) de um derivado de tetrazoliloxima |
| JP6010214B2 (ja) * | 2013-03-05 | 2016-10-19 | 日本曹達株式会社 | リゾープス属菌またはフザリウム属菌を防除する方法 |
| WO2017018409A1 (ja) * | 2015-07-28 | 2017-02-02 | 日本曹達株式会社 | ピリジン－２－イルピリジニウム化合物およびその使用方法 |
| WO2018069109A1 (en) | 2016-10-10 | 2018-04-19 | Basf Se | Pesticidal mixtures |
| US20190307127A1 (en) | 2016-10-10 | 2019-10-10 | Basf Se | Pesticidal Mixtures |
| WO2018069110A1 (en) | 2016-10-10 | 2018-04-19 | Basf Se | Pesticidal mixtures |
| AU2020226609B2 (en) | 2019-02-20 | 2025-07-24 | Basf Se | Pesticidal mixtures comprising a pyrazole compound |
| CN112110911B (zh) * | 2019-06-19 | 2024-04-26 | 东莞市东阳光农药研发有限公司 | 1,3,4-噁二唑类肟衍生物及其制备方法和应用 |
| KR102345734B1 (ko) | 2019-06-21 | 2021-12-31 | 주식회사 라파스 | 최소 침습적 바이오 센싱을 위한 생체적합성이고 전기전도성인 고분자 마이크로니들 바이오 센서 |
| CN112979633B (zh) * | 2019-12-12 | 2024-02-02 | 东莞市东阳光农药研发有限公司 | 新的肟类衍生物及其制备方法和应用 |
| CN112979628B (zh) * | 2019-12-12 | 2024-04-26 | 东莞市东阳光农药研发有限公司 | 二苯醚取代的肟类衍生物及其在农业中的应用 |
| CN114685392A (zh) * | 2020-12-28 | 2022-07-01 | 东莞市东阳光农药研发有限公司 | 一种苯基-四唑肟类衍生物及其制备方法和应用 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2581063B1 (fr) * | 1985-04-30 | 1987-07-17 | Chauvin Blache Lab | Amino-2 thiazoles n-substitues, leur procede de preparation et leur application en therapeutique |
| US4933355A (en) * | 1988-04-14 | 1990-06-12 | Sankyo Company Limited | Thiazole derivatives, their preparation and their use in the treatment of diabetes complications |
| FR2687149B1 (fr) * | 1992-02-12 | 1995-11-03 | Roussel Uclaf | Nouveaux esters pyrethrinouides derives d'alcools thiazoliques, leur procede de preparation et leur application comme pesticides. |
| US5455351A (en) * | 1993-12-13 | 1995-10-03 | Abbott Laboratories | Retroviral protease inhibiting piperazine compounds |
| KR100369753B1 (ko) * | 1997-12-10 | 2003-02-12 | 다이니혼 잉키 가가쿠 고교 가부시키가이샤 | 옥심유도체 및 이를 함유하는 농약 |
| US6472386B1 (en) * | 2001-06-29 | 2002-10-29 | Kowa Co., Ltd. | Cyclic diamine compound with 5-membered ring groups |
| AR035087A1 (es) * | 2001-08-09 | 2004-04-14 | Syngenta Participations Ag | Piridil-alquinos y piridil-n-oxido-alquinos herbicidas activos, procedimiento para su preparacion, composicion herbicida y para inhibir el crecimiento de plantas, metodo para el control del crecimiento de plantas indeseables , y metodo para la inhibicion del crecimiento de plantas |
| US7183299B2 (en) * | 2001-08-20 | 2007-02-27 | Nippon Soda Co., Ltd. | Tetrazoyl oxime derivative and agricultural chemical containing the same as active ingredient |
| JP4330313B2 (ja) * | 2001-08-20 | 2009-09-16 | 日本曹達株式会社 | テトラゾイルオキシム誘導体及びこれを有効成分とする農薬 |
| AR037754A1 (es) | 2001-12-11 | 2004-12-01 | Syngenta Participations Ag | Herbicidas |
| JP2004131392A (ja) | 2002-10-08 | 2004-04-30 | Sumitomo Chem Co Ltd | テトラゾール化合物およびその用途 |
| JP2004131416A (ja) * | 2002-10-10 | 2004-04-30 | Sumitomo Chem Co Ltd | テトラゾール化合物およびその植物病害防除用途 |
| JP2007502298A (ja) | 2003-08-14 | 2007-02-08 | スミスクライン ビーチャム コーポレーション | 化合物 |
| DE102004016845A1 (de) | 2004-04-07 | 2005-10-27 | Bayer Healthcare Ag | Phenylthioessigsäure-Derivate und ihre Verwendung |
| TWI346109B (en) * | 2004-04-30 | 2011-08-01 | Otsuka Pharma Co Ltd | 4-amino-5-cyanopyrimidine derivatives |
| US8129415B2 (en) * | 2006-07-13 | 2012-03-06 | Bayer Cropscience Ag | Fungicide hydroximoyl-tetrazole derivatives |
| KR20090033436A (ko) * | 2006-07-13 | 2009-04-03 | 바이엘 크롭사이언스 소시에떼아노님 | 살진균제 히드록시모일-테트라졸 유도체 |
| BRPI0712275A2 (pt) * | 2006-07-13 | 2012-01-10 | Bayer Cropscience Sa | composto, composição fungicida, uso de composto e método de controle curativo ou preventivo dos fungos fitopatogênicos de plantas ou culturas |
| US8084613B2 (en) * | 2007-05-14 | 2011-12-27 | Nippon Soda Co., Ltd. | Tetrazoyloxime derivative and plant disease control agent |
| KR20100029843A (ko) | 2007-08-08 | 2010-03-17 | 닛뽕소다 가부시키가이샤 | 테트라조일옥심 유도체 및 식물 병해 방제제 |
| KR20100107047A (ko) * | 2008-01-16 | 2010-10-04 | 바이엘 크롭사이언스 아게 | 살진균제 히드록시모일-테트라졸 유도체 |
-
2009
- 2009-03-18 WO PCT/EP2009/053208 patent/WO2009115557A2/en not_active Ceased
- 2009-03-18 EP EP09721227A patent/EP2265118A2/en not_active Withdrawn
- 2009-03-18 BR BRPI0906023-5A patent/BRPI0906023A2/pt not_active IP Right Cessation
- 2009-03-18 US US12/933,276 patent/US8466176B2/en not_active Expired - Fee Related
- 2009-03-18 CN CN200980109889.4A patent/CN101977504B/zh not_active Expired - Fee Related
- 2009-03-18 JP JP2011500217A patent/JP5571062B2/ja not_active Expired - Fee Related
- 2009-03-18 KR KR1020107023225A patent/KR20100125424A/ko not_active Withdrawn
- 2009-03-18 MX MX2010010135A patent/MX2010010135A/es active IP Right Grant
-
2010
- 2010-09-02 ZA ZA2010/06312A patent/ZA201006312B/en unknown
- 2010-09-15 CO CO10114368A patent/CO6280584A2/es not_active Application Discontinuation
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2011520778A5 (enExample) | ||
| AU2021297861B2 (en) | Triazine benzoate compound and application thereof | |
| ES2558166T3 (es) | Compuestos de N-tio-antranilamida y su uso como pesticidas | |
| DE69410894T2 (de) | 2-Aminothiazolcarboxamid Derivate, Verfahren zu deren Herstellung und deren Verwendung zur Bekämpfung von phytopathogenen Organismen | |
| HUP0102415A2 (hu) | Oximszármazékok, intermedierjeik, előállításuk és a vegyületeket tartalmazó mezőgazdasági növényvédő szerek | |
| RU2010107171A (ru) | Фунгицидные n-циклоалкилбензилтиокарбоксамиды или n-циклоалкилбензил-n, -замещенные амидиновые производные | |
| RU2008135317A (ru) | Фунгицидные -циклоалкилбензиламидные производные | |
| WO2020063756A1 (en) | Triazole compound and use thereof in agriculture | |
| JP2010534716A5 (enExample) | ||
| MD4264B1 (en) | Pyrazole compound, process for its production and herbicide containing it | |
| CN104876922A (zh) | 一类芳氧苯氧丙酸酰胺类除草剂 | |
| JP2008280344A (ja) | ヒドラジド化合物及びそれを含有する有害節足動物防除剤 | |
| JP2025539307A (ja) | オキサジアゾロン類化合物、除草組成物及びその用途 | |
| CN110818699B (zh) | 一种异恶唑啉类化合物及其用途 | |
| CN113831299B (zh) | 苯甲酸酯类化合物及其应用 | |
| BRPI0617777A2 (pt) | composto de amida, composição, método para controlar doenças de plantas e uso | |
| CN110914261B (zh) | 噁二唑类肟衍生物及其在农业中的应用 | |
| CN101407490B (zh) | 3-苯甲酸基丙烯酸酯类化合物及其应用 | |
| CN1749236A (zh) | 一种芳氧苯甲酸1,2二取代烯丙酯类化合物及其应用 | |
| CN113831298B (zh) | 光活性羧酸酯类化合物及其应用 | |
| CN105906618B (zh) | N-(5-苄基噻唑-2-基)-2-[4-(喹喔啉-2-氧基)苯氧基]酰胺衍生物 | |
| JP2005263639A (ja) | ５員複素環を有するアミド化合物とその用途 | |
| AR073049A1 (es) | Derivados fungicidas de oxialquilamida | |
| CN110396083A (zh) | 含哒嗪酮基丁烯内酯类化合物及其用途 | |
| CN108610283B (zh) | 一种仲胺类化合物及其制备和应用 |