JP2018533550A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2018533550A5 JP2018533550A5 JP2018515440A JP2018515440A JP2018533550A5 JP 2018533550 A5 JP2018533550 A5 JP 2018533550A5 JP 2018515440 A JP2018515440 A JP 2018515440A JP 2018515440 A JP2018515440 A JP 2018515440A JP 2018533550 A5 JP2018533550 A5 JP 2018533550A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- haloalkyl
- alkyl
- halogen
- formula
- 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.)
- Abandoned
Links
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 54
- 229910052736 halogen Inorganic materials 0.000 claims description 46
- 150000002367 halogens Chemical class 0.000 claims description 46
- 150000001875 compounds Chemical class 0.000 claims description 38
- 229910052739 hydrogen Inorganic materials 0.000 claims description 38
- 239000001257 hydrogen Substances 0.000 claims description 38
- 125000000217 alkyl group Chemical group 0.000 claims description 37
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 30
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 24
- 125000004770 (C1-C4) haloalkylsulfanyl group Chemical group 0.000 claims description 20
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 claims description 20
- 150000002431 hydrogen Chemical class 0.000 claims description 20
- -1 phenylcarbonyl thio, cyano, mercapto Chemical class 0.000 claims description 20
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 19
- 125000001424 substituent group Chemical group 0.000 claims description 19
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 16
- 125000004122 cyclic group Chemical group 0.000 claims description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 12
- 125000001188 haloalkyl group Chemical group 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 9
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 125000004740 (C1-C6) haloalkylsulfanyl group Chemical group 0.000 claims description 6
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims description 6
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims description 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 6
- 241000607479 Yersinia pestis Species 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 5
- 229910052717 sulfur Chemical group 0.000 claims description 5
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Chemical group 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000011593 sulfur Chemical group 0.000 claims description 4
- 125000004434 sulfur atom Chemical group 0.000 claims description 4
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 3
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 2
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims description 2
- YXVPOZGHMRTKCF-UHFFFAOYSA-N 1-methyl-3-(2-methylsulfanylphenyl)-5-[2-(trifluoromethyl)phenyl]-1,2,4-triazole Chemical compound CSC1=CC=CC=C1C1=NN(C)C(C=2C(=CC=CC=2)C(F)(F)F)=N1 YXVPOZGHMRTKCF-UHFFFAOYSA-N 0.000 claims description 2
- VEUMBMHMMCOFAG-UHFFFAOYSA-N 2,3-dihydrooxadiazole Chemical compound N1NC=CO1 VEUMBMHMMCOFAG-UHFFFAOYSA-N 0.000 claims description 2
- SHRIWOKJRAZPAH-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-5-[2-(methylthio)phenyl]-1,3,4-oxadiazole Chemical compound CSC1=CC=CC=C1C1=NN=C(C=2C(=CC(Cl)=CC=2)Cl)O1 SHRIWOKJRAZPAH-UHFFFAOYSA-N 0.000 claims description 2
- GAVUVVDBUKSDOY-UHFFFAOYSA-N 2-(4-bromophenyl)-5-(2-methylsulfanylphenyl)-1,3,4-oxadiazole Chemical compound CSC1=CC=CC=C1C1=NN=C(C=2C=CC(Br)=CC=2)O1 GAVUVVDBUKSDOY-UHFFFAOYSA-N 0.000 claims description 2
- RMRBSSOHCXDSMX-UHFFFAOYSA-N 2-(4-fluorophenyl)-5-(2-methylsulfanylphenyl)-1,3,4-oxadiazole Chemical compound CSC1=CC=CC=C1C1=NN=C(C=2C=CC(F)=CC=2)O1 RMRBSSOHCXDSMX-UHFFFAOYSA-N 0.000 claims description 2
- YZIKWDWSWBFFMH-UHFFFAOYSA-N 2-[1-(2-methylsulfanylphenyl)triazol-4-yl]pyridine Chemical compound CSC1=C(C=CC=C1)N1N=NC(=C1)C1=NC=CC=C1 YZIKWDWSWBFFMH-UHFFFAOYSA-N 0.000 claims description 2
- PWLHEUHTRSRRJR-UHFFFAOYSA-N 4-phenyl-1-[2-(trifluoromethylsulfanyl)phenyl]triazole Chemical compound C1(=CC=CC=C1)C=1N=NN(C=1)C1=C(C=CC=C1)SC(F)(F)F PWLHEUHTRSRRJR-UHFFFAOYSA-N 0.000 claims description 2
- BNDBBMBRXMBDGH-UHFFFAOYSA-N 5-(2-methylsulfanylphenyl)-3-phenyl-1h-1,2,4-triazole Chemical compound CSC1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=NN1 BNDBBMBRXMBDGH-UHFFFAOYSA-N 0.000 claims description 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 2
- ZQIITVMXGAETAX-UHFFFAOYSA-N CSC1=C(C=CC=C1)N1N=NC(=C1)C1=CC=CC=C1 Chemical compound CSC1=C(C=CC=C1)N1N=NC(=C1)C1=CC=CC=C1 ZQIITVMXGAETAX-UHFFFAOYSA-N 0.000 claims description 2
- 150000001204 N-oxides Chemical class 0.000 claims description 2
- 239000012752 auxiliary agent Substances 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 239000012634 fragment Substances 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000002950 monocyclic group Chemical group 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 230000000361 pesticidal effect Effects 0.000 claims 1
- 0 *C1=**=**[*-]1 Chemical compound *C1=**=**[*-]1 0.000 description 15
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 description 10
- 125000003545 alkoxy group Chemical group 0.000 description 9
- 125000004414 alkyl thio group Chemical group 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 2
- 125000004438 haloalkoxy group Chemical group 0.000 description 2
- RSMUEVVDWZBOAM-UHFFFAOYSA-N 2-(3,4-dichlorophenyl)-5-(2-methylsulfanylphenyl)-1,3,4-oxadiazole Chemical compound CSC1=CC=CC=C1C1=NN=C(C=2C=C(Cl)C(Cl)=CC=2)O1 RSMUEVVDWZBOAM-UHFFFAOYSA-N 0.000 description 1
- APANUNPEOBVFCB-UHFFFAOYSA-N C/C(/NC)=N/[NH+]=[NH2+] Chemical compound C/C(/NC)=N/[NH+]=[NH2+] APANUNPEOBVFCB-UHFFFAOYSA-N 0.000 description 1
- VEOBELAUIVEIRB-UHFFFAOYSA-N CCc1nc(C)n[o]1 Chemical compound CCc1nc(C)n[o]1 VEOBELAUIVEIRB-UHFFFAOYSA-N 0.000 description 1
- OXCKCFJIKRGXMM-UHFFFAOYSA-N CCc1ncc(C)nc1 Chemical compound CCc1ncc(C)nc1 OXCKCFJIKRGXMM-UHFFFAOYSA-N 0.000 description 1
- HKGFHAZYWIMNAM-UHFFFAOYSA-N CCc1nnc(C)[o]1 Chemical compound CCc1nnc(C)[o]1 HKGFHAZYWIMNAM-UHFFFAOYSA-N 0.000 description 1
- MPBPVACPFBSAFW-UHFFFAOYSA-N Cc1n[s]c(C)n1 Chemical compound Cc1n[s]c(C)n1 MPBPVACPFBSAFW-UHFFFAOYSA-N 0.000 description 1
- IEYZDSWQKBBPSF-UHFFFAOYSA-N Cc1nnc(C)nc1 Chemical compound Cc1nnc(C)nc1 IEYZDSWQKBBPSF-UHFFFAOYSA-N 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 1
- 238000002405 diagnostic procedure Methods 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15186944 | 2015-09-25 | ||
| EP15186944.3 | 2015-09-25 | ||
| PCT/EP2016/072285 WO2017050751A1 (en) | 2015-09-25 | 2016-09-20 | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2018533550A JP2018533550A (ja) | 2018-11-15 |
| JP2018533550A5 true JP2018533550A5 (cg-RX-API-DMAC7.html) | 2019-10-31 |
Family
ID=54199125
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018515440A Abandoned JP2018533550A (ja) | 2015-09-25 | 2016-09-20 | 硫黄含有置換基を有する殺有害生物的に活性な複素環式誘導体 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20180213779A1 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3353160B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2018533550A (cg-RX-API-DMAC7.html) |
| CN (1) | CN108137531A (cg-RX-API-DMAC7.html) |
| BR (1) | BR112018005888A2 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2017050751A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108368064B (zh) | 2015-11-30 | 2022-04-26 | 北兴化学工业株式会社 | 1,2,3-三唑衍生物和包含这种衍生物作为活性成分的杀虫剂和杀螨剂 |
| WO2017188078A1 (ja) * | 2016-04-28 | 2017-11-02 | 住友化学株式会社 | 複素環化合物 |
| AU2018399610B2 (en) * | 2018-01-05 | 2022-11-10 | F. Hoffmann-La Roche Ag | Enhancement of nucleic acid polymerization by aromatic compounds |
| CN108218848B (zh) * | 2018-01-22 | 2020-12-18 | 贵州大学 | 一种三氟甲基吡啶联噁二唑（醚）类衍生物及其应用 |
| JP7535208B2 (ja) * | 2022-03-28 | 2024-08-15 | 日本化薬株式会社 | 有害生物防除剤 |
| AU2024235487A1 (en) | 2023-03-14 | 2025-09-25 | Syngenta Crop Protection Ag | Control of pests resistant to insecticides |
Family Cites Families (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR241530A1 (es) * | 1984-12-21 | 1992-08-31 | Ciba Geigy A G Cesionaria De F | 1,2,4-triazoles, composicion para el control de pestes y procedimiento para la preparacion de 1,2,4-triazoles. |
| BR8600161A (pt) | 1985-01-18 | 1986-09-23 | Plant Genetic Systems Nv | Gene quimerico,vetores de plasmidio hibrido,intermediario,processo para controlar insetos em agricultura ou horticultura,composicao inseticida,processo para transformar celulas de plantas para expressar uma toxina de polipeptideo produzida por bacillus thuringiensis,planta,semente de planta,cultura de celulas e plasmidio |
| CA1340685C (en) | 1988-07-29 | 1999-07-27 | Frederick Meins | Dna sequences encoding polypeptides having beta-1,3-glucanase activity |
| US5169629A (en) | 1988-11-01 | 1992-12-08 | Mycogen Corporation | Process of controlling lepidopteran pests, using bacillus thuringiensis isolate denoted b.t ps81gg |
| NZ231804A (en) | 1988-12-19 | 1993-03-26 | Ciba Geigy Ag | Insecticidal toxin from leiurus quinquestriatus hebraeus |
| DK0392225T3 (da) | 1989-03-24 | 2003-09-22 | Syngenta Participations Ag | Sygdomsresistente transgene planter |
| GB8910624D0 (en) | 1989-05-09 | 1989-06-21 | Ici Plc | Bacterial strains |
| CA2015951A1 (en) | 1989-05-18 | 1990-11-18 | Mycogen Corporation | Novel bacillus thuringiensis isolates active against lepidopteran pests, and genes encoding novel lepidopteran-active toxins |
| ES2074547T3 (es) | 1989-11-07 | 1995-09-16 | Pioneer Hi Bred Int | Lectinas larvicidas, y resistencia inducida de las plantas a los insectos. |
| US5639949A (en) | 1990-08-20 | 1997-06-17 | Ciba-Geigy Corporation | Genes for the synthesis of antipathogenic substances |
| UA48104C2 (uk) | 1991-10-04 | 2002-08-15 | Новартіс Аг | Фрагмент днк, який містить послідовність,що кодує інсектицидний протеїн, оптимізовану для кукурудзи,фрагмент днк, який забезпечує направлену бажану для серцевини стебла експресію зв'язаного з нею структурного гена в рослині, фрагмент днк, який забезпечує специфічну для пилку експресію зв`язаного з нею структурного гена в рослині, рекомбінантна молекула днк, спосіб одержання оптимізованої для кукурудзи кодуючої послідовності інсектицидного протеїну, спосіб захисту рослин кукурудзи щонайменше від однієї комахи-шкідника |
| US5530195A (en) | 1994-06-10 | 1996-06-25 | Ciba-Geigy Corporation | Bacillus thuringiensis gene encoding a toxin active against insects |
| US5631072A (en) | 1995-03-10 | 1997-05-20 | Avondale Incorporated | Method and means for increasing efficacy and wash durability of insecticide treated fabric |
| ES2244214T3 (es) | 1998-09-15 | 2005-12-01 | Syngenta Participations Ag | Piridincetonas utiles como herbicidas. |
| US6413992B1 (en) * | 1998-10-23 | 2002-07-02 | Dow Agrosciences Llc | 3-(substituted pyridyl)-1,2,4-triazole compounds |
| US6518266B1 (en) * | 1999-07-22 | 2003-02-11 | 3-Dimensional Pharmaceuticals | 1- Aryl-3-thioalkyl pyrazoles, the synthesis thereof and the use thereof as insecticides |
| WO2002015701A2 (en) | 2000-08-25 | 2002-02-28 | Syngenta Participations Ag | Bacillus thuringiensis crystal protein hybrids |
| BR0209499A (pt) * | 2001-05-09 | 2004-07-06 | Sumitomo Chem Takeda Agro Co | Composto, processo para produzir o composto, e, composição pesticida |
| WO2003000906A2 (en) | 2001-06-22 | 2003-01-03 | Syngenta Participations Ag | Plant disease resistance genes |
| US7230167B2 (en) | 2001-08-31 | 2007-06-12 | Syngenta Participations Ag | Modified Cry3A toxins and nucleic acid sequences coding therefor |
| DE60205767D1 (de) | 2001-10-25 | 2005-09-29 | Siamdutch Mosquito Netting Co | Behandlung von geweben mit einem insektizid |
| AU2002361696A1 (en) | 2001-12-17 | 2003-06-30 | Syngenta Participations Ag | Novel corn event |
| US20050132500A1 (en) | 2003-12-22 | 2005-06-23 | Basf Aktiengesellschaft | Composition for impregnation of fibers, fabrics and nettings imparting a protective activity against pests |
| KR100963370B1 (ko) | 2004-02-18 | 2010-06-14 | 이시하라 산교 가부시끼가이샤 | 안트라닐아미드계 화합물, 그의 제조 방법 및 그것을함유하는 유해 생물 방제제 |
| DE102004023894A1 (de) | 2004-05-12 | 2005-12-08 | Basf Ag | Verfahren zur Behandlung von flexiblen Substraten |
| DE102005007160A1 (de) | 2005-02-16 | 2006-08-24 | Basf Ag | Pyrazolcarbonsäureanilide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen |
| DE102005020889A1 (de) | 2005-05-04 | 2006-11-09 | Fritz Blanke Gmbh & Co.Kg | Verfahren zur antimikrobiellen Ausrüstung von textilen Flächengebilden |
| MX2007015020A (es) | 2005-06-03 | 2008-01-17 | Basf Ag | Composicion para la impregnacion de fibras, telas y mallas que comparte una actividad protectora contra plagas. |
| CA2621228C (en) | 2005-09-02 | 2014-05-27 | Nissan Chemical Industries, Ltd. | Isoxazoline-substituted benzamide compound and pesticide |
| US7732469B2 (en) | 2005-10-25 | 2010-06-08 | Syngenta Crop Protection, Inc. | Heterocyclic amide derivatives useful as microbiocides |
| EP1984555B1 (de) | 2006-02-03 | 2016-05-11 | Basf Se | Verfahren zum behandeln von textilen substraten |
| DE102007003036A1 (de) * | 2006-12-20 | 2008-06-26 | Bayer Cropscience Ag | Pyrimidinylpyrazole |
| JP5230731B2 (ja) | 2007-06-12 | 2013-07-10 | ビーエーエスエフ ソシエタス・ヨーロピア | 害虫からの保護活性を付与するための非生物材料への含浸用水性製剤及び含浸方法 |
| BRPI0818332A2 (pt) | 2008-11-25 | 2018-10-30 | Qin Zhaohai | hidrocarbilideno nitrohidrozinacarboximidamidas e método para fazer as mesmas, assim como seu uso como inseticida |
| US8273764B2 (en) | 2009-04-28 | 2012-09-25 | Sumitomo Chemical Company, Limited | Fused heterocyclic compounds and use thereof |
| TWI528899B (zh) | 2010-12-29 | 2016-04-11 | 杜邦股份有限公司 | 中離子性殺蟲劑 |
| TWI545119B (zh) | 2011-08-04 | 2016-08-11 | 住友化學股份有限公司 | 稠合雜環化合物及其在病蟲害防制上之用途 |
| TW201418223A (zh) * | 2012-10-25 | 2014-05-16 | Du Pont | 經取代之甲苯基殺真菌劑 |
| WO2014102245A1 (en) * | 2012-12-27 | 2014-07-03 | Basf Se | Cyano-substituted 2-(pyridin-3-yl)-5-hetaryl-thiazole compounds for combating invertebrate pests |
| LT3066080T (lt) * | 2013-11-05 | 2018-09-10 | Bayer Cropscience Aktiengesellschaft | Nauji junginiai kovai su artropodais |
| BR112016022043B1 (pt) * | 2014-03-28 | 2020-12-29 | Syngenta Participations Ag | compostos, composição pesticida, método para controle de pragas e método para a proteção de material de propagação de plantas do ataque por pragas |
| CN106488914B (zh) * | 2014-03-28 | 2019-05-14 | 先正达参股股份有限公司 | 具有含硫取代基的具杀有害生物活性杂环衍生物 |
| JP6493394B2 (ja) * | 2014-04-24 | 2019-04-03 | 住友化学株式会社 | ジアリール−アゾール化合物 |
| EP3766871A1 (en) | 2014-08-13 | 2021-01-20 | Nippon Soda Co., Ltd. | Diarylimidazole compound and pest control agent |
| US10293391B2 (en) * | 2015-03-31 | 2019-05-21 | Nucor Corporation | Coil sampling stand and method of taking coil samples |
| EP3805213A3 (en) * | 2015-06-18 | 2021-06-09 | Nippon Soda Co., Ltd. | 1-(2-(ethylsulfonyl)-phenyl)-4-(phenyl)-1h-1,2,3-triazole and 4-(2-(ethylsulfonyl)-phenyl)-1-(phenyl)-1h-1,2,3-triazole and related compounds derivatives as pesticides |
| US10512265B2 (en) * | 2015-07-24 | 2019-12-24 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| EP3353173B1 (en) * | 2015-09-25 | 2021-07-21 | Syngenta Participations AG | Pesticidally active polycyclic derivatives with 5-membered sulfur containing heterocyclic ring systems |
| EP3356343B1 (en) * | 2015-09-28 | 2020-03-18 | Syngenta Participations AG | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
-
2016
- 2016-09-20 CN CN201680055163.7A patent/CN108137531A/zh active Pending
- 2016-09-20 EP EP16767288.0A patent/EP3353160B1/en active Active
- 2016-09-20 US US15/762,998 patent/US20180213779A1/en not_active Abandoned
- 2016-09-20 BR BR112018005888A patent/BR112018005888A2/pt not_active Application Discontinuation
- 2016-09-20 WO PCT/EP2016/072285 patent/WO2017050751A1/en not_active Ceased
- 2016-09-20 JP JP2018515440A patent/JP2018533550A/ja not_active Abandoned