JP2010138159A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2010138159A5 JP2010138159A5 JP2009155522A JP2009155522A JP2010138159A5 JP 2010138159 A5 JP2010138159 A5 JP 2010138159A5 JP 2009155522 A JP2009155522 A JP 2009155522A JP 2009155522 A JP2009155522 A JP 2009155522A JP 2010138159 A5 JP2010138159 A5 JP 2010138159A5
- Authority
- JP
- Japan
- Prior art keywords
- methylbenzoyl
- trimethoxy
- group
- chloro
- methoxypyridine
- 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
- 125000003545 alkoxy group Chemical group 0.000 claims 14
- 230000000855 fungicidal effect Effects 0.000 claims 13
- 125000000217 alkyl group Chemical group 0.000 claims 11
- GCSHUYKULREZSJ-UHFFFAOYSA-N phenyl(pyridin-2-yl)methanone Chemical class C=1C=CC=NC=1C(=O)C1=CC=CC=C1 GCSHUYKULREZSJ-UHFFFAOYSA-N 0.000 claims 9
- 125000005843 halogen group Chemical group 0.000 claims 8
- -1 off Ruthianyl Chemical compound 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 7
- 125000004414 alkyl thio group Chemical group 0.000 claims 6
- 239000000417 fungicide Substances 0.000 claims 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- PFFIDZXUXFLSSR-UHFFFAOYSA-N 1-methyl-N-[2-(4-methylpentan-2-yl)-3-thienyl]-3-(trifluoromethyl)pyrazole-4-carboxamide Chemical compound S1C=CC(NC(=O)C=2C(=NN(C)C=2)C(F)(F)F)=C1C(C)CC(C)C PFFIDZXUXFLSSR-UHFFFAOYSA-N 0.000 claims 3
- 239000005740 Boscalid Substances 0.000 claims 3
- 239000005760 Difenoconazole Substances 0.000 claims 3
- 239000005816 Penthiopyrad Substances 0.000 claims 3
- 239000005869 Pyraclostrobin Substances 0.000 claims 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 3
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 claims 3
- 229940118790 boscalid Drugs 0.000 claims 3
- 239000000645 desinfectant Substances 0.000 claims 3
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 claims 3
- CRFYLQMIDWBKRT-LPYMAVHISA-N pyribencarb Chemical compound C1=C(Cl)C(CNC(=O)OC)=CC(C(\C)=N\OCC=2N=C(C)C=CC=2)=C1 CRFYLQMIDWBKRT-LPYMAVHISA-N 0.000 claims 3
- NMVCBWZLCXANER-UHFFFAOYSA-N pyriofenone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(Cl)=CN=C1OC NMVCBWZLCXANER-UHFFFAOYSA-N 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 239000011593 sulfur Substances 0.000 claims 3
- ZHBRLEQONSVJJN-UHFFFAOYSA-N [2,5-dichloro-3-(trifluoromethyl)pyridin-4-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical group COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(Cl)C=NC(Cl)=C1C(F)(F)F ZHBRLEQONSVJJN-UHFFFAOYSA-N 0.000 claims 2
- KKJKGRYXBURLSH-UHFFFAOYSA-N [2-chloro-5-methoxy-3-(trifluoromethyl)pyridin-4-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=CN=C(Cl)C(C(F)(F)F)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC KKJKGRYXBURLSH-UHFFFAOYSA-N 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- VRAOJYRJSZMFNB-UHFFFAOYSA-N (2,3,5-trichloropyridin-4-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(Cl)C=NC(Cl)=C1Cl VRAOJYRJSZMFNB-UHFFFAOYSA-N 0.000 claims 1
- QVBJZYHGMQEEDY-UHFFFAOYSA-N (2,4-dichloro-5-iodopyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(Cl)N=CC(I)=C1Cl QVBJZYHGMQEEDY-UHFFFAOYSA-N 0.000 claims 1
- WAKQYZHLOFWXJU-UHFFFAOYSA-N (2,4-dichloro-5-methylpyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(Cl)N=CC(C)=C1Cl WAKQYZHLOFWXJU-UHFFFAOYSA-N 0.000 claims 1
- LTKQGTWYXRAHOI-UHFFFAOYSA-N (2-ethoxy-3,4-dimethoxy-6-methylphenyl)-(2-ethoxy-4,5-dimethylpyridin-3-yl)methanone Chemical compound CCOC1=NC=C(C)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OCC LTKQGTWYXRAHOI-UHFFFAOYSA-N 0.000 claims 1
- QJWVWMJDSFGHDD-UHFFFAOYSA-N (2-fluoro-4-iodo-5-methylpyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(F)N=CC(C)=C1I QJWVWMJDSFGHDD-UHFFFAOYSA-N 0.000 claims 1
- WQPCBHYGDPBVEL-UHFFFAOYSA-N (2-methoxy-4,5-dimethylpyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(C)=CN=C1OC WQPCBHYGDPBVEL-UHFFFAOYSA-N 0.000 claims 1
- RBSJWOHHMGUIAP-UHFFFAOYSA-N (3,5-dichloropyridin-4-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(Cl)C=NC=C1Cl RBSJWOHHMGUIAP-UHFFFAOYSA-N 0.000 claims 1
- LMKQFVSKNKSIAN-UHFFFAOYSA-N (3-bromo-5-methylpyridin-4-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C=NC=C1Br LMKQFVSKNKSIAN-UHFFFAOYSA-N 0.000 claims 1
- FKEQCEOADLXPAU-UHFFFAOYSA-N (3-chloro-5-methoxypyridin-4-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=CN=CC(Cl)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC FKEQCEOADLXPAU-UHFFFAOYSA-N 0.000 claims 1
- FCBIWFPVBUYMEG-UHFFFAOYSA-N (4,5-dibromo-2-methoxypyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(Br)=C1Br FCBIWFPVBUYMEG-UHFFFAOYSA-N 0.000 claims 1
- SXEDMKXHMMJEPN-UHFFFAOYSA-N (4,5-dichloro-2-methoxypyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(Cl)=C1Cl SXEDMKXHMMJEPN-UHFFFAOYSA-N 0.000 claims 1
- NIURNYYMOATFBR-UHFFFAOYSA-N (4,5-dichloro-2-methoxypyridin-3-yl)-(4,5-dimethoxy-2-methylphenyl)methanone Chemical compound C1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(Cl)=C1Cl NIURNYYMOATFBR-UHFFFAOYSA-N 0.000 claims 1
- HXMOJVGNCHVMML-UHFFFAOYSA-N (4,5-dichloro-2-methoxypyridin-3-yl)-(5-ethoxy-4-methoxy-2-methylphenyl)methanone Chemical compound C1=C(OC)C(OCC)=CC(C(=O)C=2C(=NC=C(Cl)C=2Cl)OC)=C1C HXMOJVGNCHVMML-UHFFFAOYSA-N 0.000 claims 1
- UXLYZENZVLYOFG-UHFFFAOYSA-N (4-bromo-5-chloro-2-ethoxypyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound CCOC1=NC=C(Cl)C(Br)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC UXLYZENZVLYOFG-UHFFFAOYSA-N 0.000 claims 1
- SYYSCNWMIXCLGX-UHFFFAOYSA-N (4-bromo-5-chloro-2-methoxypyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(Br)C(Cl)=CN=C1OC SYYSCNWMIXCLGX-UHFFFAOYSA-N 0.000 claims 1
- YMXSVKQINKVKFY-UHFFFAOYSA-N (4-chloro-2-methoxy-5-methylpyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(C)=C1Cl YMXSVKQINKVKFY-UHFFFAOYSA-N 0.000 claims 1
- LQDAXAVAUVYWPU-UHFFFAOYSA-N (4-chloro-5-iodo-2-methoxypyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(Cl)C(I)=CN=C1OC LQDAXAVAUVYWPU-UHFFFAOYSA-N 0.000 claims 1
- YFMWDDYFQBKXAF-UHFFFAOYSA-N (5-bromo-4-chloro-2-ethoxypyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound CCOC1=NC=C(Br)C(Cl)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC YFMWDDYFQBKXAF-UHFFFAOYSA-N 0.000 claims 1
- HBOCCKCCPBHTBS-UHFFFAOYSA-N (5-chloro-2,4-dimethoxypyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(Cl)=C1OC HBOCCKCCPBHTBS-UHFFFAOYSA-N 0.000 claims 1
- DNQMHEUVDCPKOG-UHFFFAOYSA-N (5-chloro-2-ethoxy-4-methylpyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound CCOC1=NC=C(Cl)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC DNQMHEUVDCPKOG-UHFFFAOYSA-N 0.000 claims 1
- OXIIBNJIJJXVBY-UHFFFAOYSA-N (5-chloro-4-ethynyl-2-methoxypyridin-3-yl)-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(Cl)=C1C#C OXIIBNJIJJXVBY-UHFFFAOYSA-N 0.000 claims 1
- HGRXBKDKSYDWLD-UHFFFAOYSA-N 2-methoxy-4-methylpyridine Chemical compound COC1=CC(C)=CC=N1 HGRXBKDKSYDWLD-UHFFFAOYSA-N 0.000 claims 1
- IWTFOFMTUOBLHG-UHFFFAOYSA-N 2-methoxypyridine Chemical compound COC1=CC=CC=N1 IWTFOFMTUOBLHG-UHFFFAOYSA-N 0.000 claims 1
- HAAJMXYZGGVOQU-UHFFFAOYSA-N COC1=C(C(=O)C=2C(=NC=C(C2Cl)Br)OC)C(=CC(=C1OC)OC)C.COC1=C(C(=O)C=2C(=NC=C(C2C)C)SC)C(=CC(=C1OC)OC)C Chemical compound COC1=C(C(=O)C=2C(=NC=C(C2Cl)Br)OC)C(=CC(=C1OC)OC)C.COC1=C(C(=O)C=2C(=NC=C(C2C)C)SC)C(=CC(=C1OC)OC)C HAAJMXYZGGVOQU-UHFFFAOYSA-N 0.000 claims 1
- CPPAIPOHJHVLMB-UHFFFAOYSA-N COC1=C(C(=O)C=2C(=NC=C(C2SC)Cl)OC)C(=CC(=C1OC)OC)C.COC1=C(C(=O)C=2C(=NC=C(C2OC)I)OC)C(=CC(=C1OC)OC)C Chemical compound COC1=C(C(=O)C=2C(=NC=C(C2SC)Cl)OC)C(=CC(=C1OC)OC)C.COC1=C(C(=O)C=2C(=NC=C(C2OC)I)OC)C(=CC(=C1OC)OC)C CPPAIPOHJHVLMB-UHFFFAOYSA-N 0.000 claims 1
- GNOHDNLDBKXZQT-UHFFFAOYSA-N [2,4-dichloro-5-(trifluoromethyl)pyridin-3-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(Cl)N=CC(C(F)(F)F)=C1Cl GNOHDNLDBKXZQT-UHFFFAOYSA-N 0.000 claims 1
- SVUHXTAXAPIIOI-UHFFFAOYSA-N [2-bromo-5-methoxy-3-(trifluoromethyl)pyridin-4-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=CN=C(Br)C(C(F)(F)F)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC SVUHXTAXAPIIOI-UHFFFAOYSA-N 0.000 claims 1
- WXANTZZBMGYAPK-UHFFFAOYSA-N [2-chloro-4-methyl-5-(trifluoromethyl)pyridin-3-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(C(F)(F)F)=CN=C1Cl WXANTZZBMGYAPK-UHFFFAOYSA-N 0.000 claims 1
- DMSGLRSHSCWAQH-UHFFFAOYSA-N [2-methoxy-4-methyl-5-(trifluoromethyl)pyridin-3-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(C)C(C(F)(F)F)=CN=C1OC DMSGLRSHSCWAQH-UHFFFAOYSA-N 0.000 claims 1
- ZRTJCTGXNYPZKL-UHFFFAOYSA-N [2-methoxy-5-methyl-4-(trifluoromethyl)pyridin-3-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(C)=C1C(F)(F)F ZRTJCTGXNYPZKL-UHFFFAOYSA-N 0.000 claims 1
- USFNNNFVYMHLOG-UHFFFAOYSA-N [4-(fluoromethyl)-2-methoxy-5-methylpyridin-3-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(C)=C1CF USFNNNFVYMHLOG-UHFFFAOYSA-N 0.000 claims 1
- SJJVVTACNTYGIF-UHFFFAOYSA-N [4-chloro-2-methoxy-5-(trifluoromethyl)pyridin-3-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(Cl)C(C(F)(F)F)=CN=C1OC SJJVVTACNTYGIF-UHFFFAOYSA-N 0.000 claims 1
- LUFSLQUGNAQUJV-UHFFFAOYSA-N [5-bromo-2-methoxy-4-(trifluoromethyl)pyridin-3-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(Br)=C1C(F)(F)F LUFSLQUGNAQUJV-UHFFFAOYSA-N 0.000 claims 1
- LVOPMINLOZBVMK-UHFFFAOYSA-N [5-bromo-4-(fluoromethyl)-2-methoxypyridin-3-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(Br)=C1CF LVOPMINLOZBVMK-UHFFFAOYSA-N 0.000 claims 1
- RHQLFSDLLCYKMZ-UHFFFAOYSA-N [5-chloro-4-(difluoromethyl)-2-methoxypyridin-3-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(Cl)=C1C(F)F RHQLFSDLLCYKMZ-UHFFFAOYSA-N 0.000 claims 1
- YJXYWADCDZDZGW-UHFFFAOYSA-N [5-chloro-4-(fluoromethyl)-2-methoxypyridin-3-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound COC1=C(OC)C(OC)=CC(C)=C1C(=O)C1=C(OC)N=CC(Cl)=C1CF YJXYWADCDZDZGW-UHFFFAOYSA-N 0.000 claims 1
- OOPMUQPIWUDNLK-UHFFFAOYSA-N [5-ethyl-2-methoxy-4-(trifluoromethyl)pyridin-3-yl]-(2,3,4-trimethoxy-6-methylphenyl)methanone Chemical compound CCC1=CN=C(OC)C(C(=O)C=2C(=C(OC)C(OC)=CC=2C)OC)=C1C(F)(F)F OOPMUQPIWUDNLK-UHFFFAOYSA-N 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- LWLJEQHTPVPKSJ-UHFFFAOYSA-N tebufloquin Chemical compound C1=C(C(C)(C)C)C=C2C(OC(=O)C)=C(C)C(C)=NC2=C1F LWLJEQHTPVPKSJ-UHFFFAOYSA-N 0.000 claims 1
- 0 *c(c(*)c1)cc(*)c1C(c1c(*)c(*)cnc1*)=O Chemical compound *c(c(*)c1)cc(*)c1C(c1c(*)c(*)cnc1*)=O 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009155522A JP5449887B2 (ja) | 2008-07-03 | 2009-06-30 | 殺菌剤組成物及び植物病害の防除方法 |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008174963 | 2008-07-03 | ||
| JP2008174963 | 2008-07-03 | ||
| JP2008292511 | 2008-11-14 | ||
| JP2008292511 | 2008-11-14 | ||
| JP2009155522A JP5449887B2 (ja) | 2008-07-03 | 2009-06-30 | 殺菌剤組成物及び植物病害の防除方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010138159A JP2010138159A (ja) | 2010-06-24 |
| JP2010138159A5 true JP2010138159A5 (https=) | 2012-07-12 |
| JP5449887B2 JP5449887B2 (ja) | 2014-03-19 |
Family
ID=41466400
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009155522A Active JP5449887B2 (ja) | 2008-07-03 | 2009-06-30 | 殺菌剤組成物及び植物病害の防除方法 |
Country Status (27)
| Country | Link |
|---|---|
| US (3) | US8962661B2 (https=) |
| EP (2) | EP2323487B1 (https=) |
| JP (1) | JP5449887B2 (https=) |
| KR (1) | KR20110025676A (https=) |
| CN (3) | CN105994322B (https=) |
| AR (1) | AR072464A1 (https=) |
| AU (1) | AU2009266746B2 (https=) |
| BR (2) | BR122017002275B1 (https=) |
| CA (5) | CA2729618C (https=) |
| CL (3) | CL2010001565A1 (https=) |
| CO (1) | CO6341529A2 (https=) |
| CY (1) | CY1115930T1 (https=) |
| DK (1) | DK2323487T3 (https=) |
| EC (1) | ECSP10010726A (https=) |
| ES (1) | ES2526555T3 (https=) |
| HR (1) | HRP20150052T1 (https=) |
| MA (1) | MA32428B1 (https=) |
| MX (4) | MX2010014502A (https=) |
| NZ (2) | NZ603490A (https=) |
| PH (2) | PH12014502690B1 (https=) |
| PL (1) | PL2323487T3 (https=) |
| PT (1) | PT2323487E (https=) |
| RS (1) | RS53759B1 (https=) |
| RU (1) | RU2507746C2 (https=) |
| SI (1) | SI2323487T1 (https=) |
| TW (2) | TWI547239B (https=) |
| WO (1) | WO2010002026A2 (https=) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103237451A (zh) * | 2010-12-08 | 2013-08-07 | 巴斯夫欧洲公司 | 杀真菌混合物 |
| JP5940368B2 (ja) | 2011-05-24 | 2016-06-29 | 石原産業株式会社 | 殺菌剤組成物及び植物病害の防除方法 |
| JP5940369B2 (ja) | 2011-05-27 | 2016-06-29 | 石原産業株式会社 | 植物病害の防除方法 |
| JP6013032B2 (ja) * | 2011-07-08 | 2016-10-25 | 石原産業株式会社 | 殺菌剤組成物及び植物病害の防除方法 |
| PT2796044T (pt) * | 2011-12-22 | 2016-08-29 | Sds Biotech Corp | Agente de controlo de doenças de plantas |
| JP2014015449A (ja) | 2012-06-13 | 2014-01-30 | Ishihara Sangyo Kaisha Ltd | 殺菌剤組成物及び植物病害の防除方法 |
| BR112015018158B1 (pt) * | 2013-01-30 | 2020-04-22 | Meiji Seika Pharma Co Ltd | composição química agrícola em suspensão aquosa |
| CN105076143A (zh) * | 2014-05-21 | 2015-11-25 | 深圳诺普信农化股份有限公司 | 杀菌组合物 |
| CN105076137A (zh) * | 2014-05-21 | 2015-11-25 | 深圳诺普信农化股份有限公司 | 一种杀菌组合物 |
| CN104025954A (zh) * | 2014-06-20 | 2014-09-10 | 广西壮族自治区农业科学院蔬菜研究所 | 一种预防和治疗厚皮甜瓜蔓枯病的生物方法 |
| US10172357B2 (en) | 2015-05-29 | 2019-01-08 | Ishihara Sangyo Kaisha, Ltd. | Fungicidal composition and method for controlling plant diseases |
| CN105165828B (zh) * | 2015-10-28 | 2017-05-10 | 陕西上格之路生物科学有限公司 | 一种含苯菌酮和硝苯菌酯的杀菌组合物 |
| RU2680309C1 (ru) * | 2018-02-13 | 2019-02-19 | Андрей Васильевич Кудряшов | Средство для защиты растений "Агройод" |
| CN108174856A (zh) * | 2018-02-28 | 2018-06-19 | 佛山市海力盈生物科技有限公司 | 一种含Pyriofenone和苯醚甲环唑的农药组合物 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69618370T2 (de) * | 1995-04-11 | 2002-09-26 | Mitsui Chemicals, Inc. | Substituierte Thiophenderivate und diese als aktiver Bestandteil enthaltenden Fungizide für Land- und Gartenbauwirtschaft |
| TWI252231B (en) * | 1997-04-14 | 2006-04-01 | American Cyanamid Co | Fungicidal trifluorophenyl-triazolopyrimidines |
| TW521072B (en) * | 1997-06-02 | 2003-02-21 | Meiji Seika Kaisha | 4-quinolinol derivatives and fungicides containing the same as an active ingredient used for agriculture and horticulture |
| AR029289A1 (es) * | 2000-07-05 | 2003-06-18 | Ishihara Sangyo Kaisha | Derivado de benzoilpiridina o su sal, fungicida que lo contiene como un ingrediente activo, su proceso de produccion e intermediario para producirlo |
| RU2255088C2 (ru) * | 2001-02-09 | 2005-06-27 | Исихара Сангио Кайся, Лтд. | Производное бензоилпиридина или его соль, содержащий его в качестве активного ингредиента фунгицид, способы его получения и промежуточные соединения для его получения |
| JP4373054B2 (ja) * | 2002-07-02 | 2009-11-25 | 三井化学アグロ株式会社 | 水性懸濁農薬組成物 |
| AU2003275716A1 (en) | 2002-10-31 | 2004-05-25 | Ishihara Sangyo Kaisha, Ltd. | 3-benzoyl-2,4,5-substituted pyridine derivatives or salts thereof and bactericides containing the same |
| ES2535705T3 (es) | 2003-10-31 | 2015-05-14 | Ishihara Sangyo Kaisha, Ltd. | Composición bactericida y método de control de la enfermedad de las plantas |
| CN101199274B (zh) * | 2003-10-31 | 2013-03-20 | 石原产业株式会社 | 杀菌剂组合物和植物病害的防除方法 |
| JP4918215B2 (ja) * | 2003-10-31 | 2012-04-18 | 石原産業株式会社 | 殺菌剤組成物及び植物病害の防除方法 |
| MXPA06011750A (es) | 2004-05-07 | 2007-03-26 | Basf Ag | Mezclas fungicidas para combatir patogenos del arroz. |
| GB0422400D0 (en) * | 2004-10-08 | 2004-11-10 | Syngenta Participations Ag | Fungicidal compositions |
| PL2036436T3 (pl) * | 2006-07-05 | 2018-02-28 | Ishihara Sangyo Kaisha, Ltd. | Kompozycja grzybobójcza i sposób zwalczania chorób roślin |
| DE102006055477A1 (de) * | 2006-11-24 | 2008-05-29 | Bayer Cropscience Ag | Pflanzenschutzgranulate zur Applikation auf die Blattoberfläche |
| CL2008000512A1 (es) | 2007-02-22 | 2008-08-29 | Bayer Cropscience Sa | Compuestos derivados de n-(3-fenilpropil)carboxamida; procedimiento de preparacion de dichos compuestos; composicion fungicida; y metodo para combatir de forma preventiva o curativa los hongos fitopatogenos de cultivos. |
| JP6013032B2 (ja) | 2011-07-08 | 2016-10-25 | 石原産業株式会社 | 殺菌剤組成物及び植物病害の防除方法 |
-
2009
- 2009-06-30 BR BR122017002275-0A patent/BR122017002275B1/pt active IP Right Grant
- 2009-06-30 CA CA2729618A patent/CA2729618C/en active Active
- 2009-06-30 CA CA3105364A patent/CA3105364C/en active Active
- 2009-06-30 CN CN201610356467.9A patent/CN105994322B/zh active Active
- 2009-06-30 RS RS20150036A patent/RS53759B1/sr unknown
- 2009-06-30 SI SI200931134T patent/SI2323487T1/sl unknown
- 2009-06-30 DK DK09773604.5T patent/DK2323487T3/en active
- 2009-06-30 ES ES09773604.5T patent/ES2526555T3/es active Active
- 2009-06-30 CN CN201310632181.5A patent/CN103636636B/zh active Active
- 2009-06-30 CA CA2995175A patent/CA2995175C/en active Active
- 2009-06-30 AU AU2009266746A patent/AU2009266746B2/en active Active
- 2009-06-30 CA CA3171691A patent/CA3171691C/en active Active
- 2009-06-30 CN CN200980125689.8A patent/CN102083317B/zh active Active
- 2009-06-30 RU RU2011103772/13A patent/RU2507746C2/ru active
- 2009-06-30 MX MX2010014502A patent/MX2010014502A/es active IP Right Grant
- 2009-06-30 KR KR1020107029867A patent/KR20110025676A/ko not_active Ceased
- 2009-06-30 CA CA2923126A patent/CA2923126C/en active Active
- 2009-06-30 PT PT97736045T patent/PT2323487E/pt unknown
- 2009-06-30 US US13/002,361 patent/US8962661B2/en active Active
- 2009-06-30 PL PL09773604T patent/PL2323487T3/pl unknown
- 2009-06-30 EP EP09773604.5A patent/EP2323487B1/en active Active
- 2009-06-30 JP JP2009155522A patent/JP5449887B2/ja active Active
- 2009-06-30 NZ NZ603490A patent/NZ603490A/en unknown
- 2009-06-30 MX MX2013008267A patent/MX344105B/es unknown
- 2009-06-30 EP EP12005174A patent/EP2529627A1/en not_active Withdrawn
- 2009-06-30 HR HRP20150052AT patent/HRP20150052T1/hr unknown
- 2009-06-30 MX MX2019010860A patent/MX392286B/es unknown
- 2009-06-30 NZ NZ590218A patent/NZ590218A/xx unknown
- 2009-06-30 MX MX2016015994A patent/MX368023B/es unknown
- 2009-06-30 WO PCT/JP2009/062259 patent/WO2010002026A2/en not_active Ceased
- 2009-06-30 BR BRPI0915594-5A patent/BRPI0915594B1/pt active IP Right Grant
- 2009-07-01 TW TW104116041A patent/TWI547239B/zh active
- 2009-07-01 TW TW098122281A patent/TWI495432B/zh active
- 2009-07-02 AR ARP090102472A patent/AR072464A1/es active IP Right Grant
-
2010
- 2010-12-23 CL CL2010001565A patent/CL2010001565A1/es unknown
- 2010-12-29 CO CO10163909A patent/CO6341529A2/es not_active Application Discontinuation
- 2010-12-29 EC EC2010010726A patent/ECSP10010726A/es unknown
- 2010-12-31 MA MA33476A patent/MA32428B1/fr unknown
-
2014
- 2014-12-02 PH PH12014502690A patent/PH12014502690B1/en unknown
- 2014-12-16 US US14/572,237 patent/US9474281B2/en active Active
-
2015
- 2015-01-05 CY CY20151100005T patent/CY1115930T1/el unknown
- 2015-02-25 CL CL2015000462A patent/CL2015000462A1/es unknown
-
2016
- 2016-08-15 US US15/237,194 patent/US10136643B2/en active Active
- 2016-11-08 CL CL2016002833A patent/CL2016002833A1/es unknown
-
2019
- 2019-09-09 PH PH12019502042A patent/PH12019502042A1/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2010138159A5 (https=) | ||
| AU2004279674B2 (en) | Synergistic fungicidal active substance combinations | |
| RU2011103772A (ru) | Фунгицидная композиция и способ контроля болезней растений | |
| JP2014523432A5 (https=) | ||
| WO2017025419A3 (de) | 2-(het)aryl-substituierte kondensierte heterocyclen-derivate als schädlingsbekämpfungsmittel | |
| WO2013010947A3 (en) | Pesticidal methods using substituted 3-pyridyl thiazole compounds and derivatives for combating animal pests ii | |
| NZ597597A (en) | Pesticidal compositions containing heteroaryl-n-aryl carbamate compounds | |
| JP2010534696A5 (https=) | ||
| UA108619C2 (xx) | Пестицидні композиції | |
| JP2009526798A5 (https=) | ||
| IL169527A (en) | Pyridine derivatives and process for their preparation | |
| JP2016528201A5 (https=) | ||
| HRP20250118T1 (hr) | Spojevi (hetero)arilimidazola i sredstva za suzbijanje opasnih organizama | |
| KR20130139892A (ko) | 살진균제 피라졸 | |
| JP2010540650A5 (https=) | ||
| UA115809C2 (uk) | Гербіцидно активні (алкінілфеніл)-заміщені циклічні діонові сполуки та їхні похідні | |
| WO2008138551A3 (de) | 3-(2-alkoxy-phenyl)-substituierte tetramate | |
| EP2529624A3 (en) | Substituted benzene fungicides | |
| MX2013002256A (es) | Pirazoles fungicidas y sus mezclas. | |
| JP2023182586A5 (https=) | ||
| WO2008152091A3 (en) | Pesticidal composition comprising a strigolactone derivative and an insecticide compound | |
| JP2017508719A5 (https=) | ||
| UA111869C2 (uk) | Сполуки 2-(заміщений феніл)-циклопентан-1,3-діону та їх похідні | |
| JP2013509419A5 (https=) | ||
| RU2015131110A (ru) | Производные 1-(замещенный бензоил)-5-фтор-4-имино-3-метил-3,4-дигидропиримидин-2(1h)-она |