JP2011520778A5 - - Google Patents
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- 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
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- 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 (https=) | 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 (https=) |
| EP (1) | EP2265118A2 (https=) |
| JP (1) | JP5571062B2 (https=) |
| KR (1) | KR20100125424A (https=) |
| CN (1) | CN101977504B (https=) |
| BR (1) | BRPI0906023A2 (https=) |
| CO (1) | CO6280584A2 (https=) |
| MX (1) | MX2010010135A (https=) |
| WO (1) | WO2009115557A2 (https=) |
| ZA (1) | ZA201006312B (https=) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2234489B1 (en) * | 2008-01-15 | 2017-04-12 | Bayer Intellectual Property GmbH | 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 |
| EP2265119A1 (en) * | 2008-03-19 | 2010-12-29 | Bayer CropScience AG | Fungicide hydroximoyl-tetrazole derivatives |
| JP5524200B2 (ja) * | 2008-07-04 | 2014-06-18 | バイエル・クロップサイエンス・アーゲー | 殺真菌剤ヒドロキシモイル−テトラゾール誘導体 |
| KR20110030663A (ko) * | 2008-07-04 | 2011-03-23 | 바이엘 크롭사이언스 아게 | 살진균제 히드록시모일-테트라졸 유도체 |
| 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 |
| EP2519103B1 (en) * | 2009-12-28 | 2014-08-13 | Bayer Intellectual Property GmbH | Fungicide hydroximoyl-tetrazole derivatives |
| BR122017023123B1 (pt) * | 2010-03-12 | 2018-04-24 | Nippon Soda Co., Ltd. | Método para produzir derivado de picolina halogenada |
| BR122017022932B1 (pt) | 2010-04-06 | 2018-05-15 | Nippon Soda Co., Ltd. | Método de produção de composto heterocíclico que contém nitrogênio |
| AU2014201037B9 (en) * | 2010-04-06 | 2015-11-19 | Nippon Soda Co., Ltd. | Nitrogen-containing heterocyclic compound and method for producing same |
| WO2011134911A2 (en) * | 2010-04-28 | 2011-11-03 | Bayer Cropscience Ag | Fungicide hydroximoyl-tetrazole derivatives |
| RS58401B1 (sr) * | 2010-10-07 | 2019-04-30 | Bayer Cropscience Ag | Sastav fungicida koji sadrži derivat tetrazoliloksima i derivat tiazolilpiperidina |
| WO2012117021A2 (en) * | 2011-03-03 | 2012-09-07 | Syngenta Participations Ag | Novel microbiocidal oxime ethers |
| JP5740042B2 (ja) * | 2012-03-13 | 2015-06-24 | 日本曹達株式会社 | 化合物、化合物の製造方法、及び化合物の精製方法 |
| WO2014136603A1 (ja) * | 2013-03-05 | 2014-09-12 | 日本曹達株式会社 | 卵菌類以外の植物病原性糸状菌を防除する方法 |
| CN107889486B (zh) | 2015-07-28 | 2021-07-09 | 日本曹达株式会社 | 吡啶-2-基吡啶化合物及其使用方法 |
| BR122022025232B1 (pt) | 2016-10-10 | 2023-10-31 | Basf Se | Mistura pesticida, composição pesticida, métodos para controlar pragas fitopatogênicas, para melhorar a saúde de plantas e para a proteção do material de propagação vegetal contra pragas e material de propagação vegetal |
| WO2018069110A1 (en) | 2016-10-10 | 2018-04-19 | Basf Se | Pesticidal mixtures |
| WO2018069108A1 (en) | 2016-10-10 | 2018-04-19 | Basf Se | Pesticidal mixtures |
| MX2021010111A (es) | 2019-02-20 | 2021-09-21 | Basf Se | Mezclas plaguicidas que comprenden un compuesto de pirazol. |
| 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 |
| NZ505002A (en) * | 1997-12-10 | 2001-11-30 | Dainippon Ink & Chemicals | 1,2,5-oxadiazolyl, 1,2,5-thiadiazolyl or 1,2,3-thiadiazolyl oxime derivatives substituted by another heterocyclic group useful as agricultural chemicals |
| 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 |
| 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 |
| US7183299B2 (en) * | 2001-08-20 | 2007-02-27 | Nippon Soda Co., Ltd. | Tetrazoyl oxime derivative and agricultural chemical containing the same as active ingredient |
| 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 |
| US20060205740A1 (en) | 2003-08-14 | 2006-09-14 | Reno Michael J | Chemical compounds |
| 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 |
| KR20090031619A (ko) * | 2006-07-13 | 2009-03-26 | 바이엘 크롭사이언스 소시에떼아노님 | 살진균제 히드록시모일-테트라졸 유도체 |
| MX2009000299A (es) * | 2006-07-13 | 2009-01-26 | Bayer Cropscience Sa | Derivados de hidroximoil-tetrazol fungicidas. |
| CA2653589A1 (en) * | 2006-07-13 | 2008-01-17 | Bayer Cropscience Sa | Fungicide hydroximoyl-tetrazole derivatives |
| US8084613B2 (en) | 2007-05-14 | 2011-12-27 | Nippon Soda Co., Ltd. | Tetrazoyloxime derivative and plant disease control agent |
| KR101327670B1 (ko) * | 2007-08-08 | 2013-11-08 | 닛뽕소다 가부시키가이샤 | 테트라조일옥심 유도체 및 식물 병해 방제제 |
| RU2010133984A (ru) * | 2008-01-16 | 2012-02-27 | Байер КропСайенс АГ (DE) | Фунгицидные производные гидроксимоилтетразола |
-
2009
- 2009-03-18 KR KR1020107023225A patent/KR20100125424A/ko not_active Withdrawn
- 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 JP JP2011500217A patent/JP5571062B2/ja not_active Expired - Fee Related
- 2009-03-18 MX MX2010010135A patent/MX2010010135A/es active IP Right Grant
- 2009-03-18 CN CN200980109889.4A patent/CN101977504B/zh not_active Expired - Fee Related
- 2009-03-18 US US12/933,276 patent/US8466176B2/en not_active Expired - Fee Related
-
2010
- 2010-09-02 ZA ZA2010/06312A patent/ZA201006312B/en unknown
- 2010-09-15 CO CO10114368A patent/CO6280584A2/es not_active Application Discontinuation
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