JP2018505887A5 - - Google Patents
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- JP2018505887A5 JP2018505887A5 JP2017541623A JP2017541623A JP2018505887A5 JP 2018505887 A5 JP2018505887 A5 JP 2018505887A5 JP 2017541623 A JP2017541623 A JP 2017541623A JP 2017541623 A JP2017541623 A JP 2017541623A JP 2018505887 A5 JP2018505887 A5 JP 2018505887A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- cyano
- alkyl
- independently
- ethyl
- 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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- -1 C 1 -C 4 -alkyl Chemical group 0.000 claims description 155
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 91
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 75
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 73
- 229910052801 chlorine Inorganic materials 0.000 claims description 73
- 239000000460 chlorine Substances 0.000 claims description 73
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 72
- 229910052731 fluorine Inorganic materials 0.000 claims description 72
- 239000011737 fluorine Substances 0.000 claims description 72
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 62
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 60
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 60
- 229910052794 bromium Inorganic materials 0.000 claims description 60
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 59
- 229910052739 hydrogen Inorganic materials 0.000 claims description 53
- 239000001257 hydrogen Substances 0.000 claims description 53
- 229910052760 oxygen Inorganic materials 0.000 claims description 35
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 28
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 24
- 150000003839 salts Chemical class 0.000 claims description 24
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 22
- 229910052717 sulfur Chemical group 0.000 claims description 22
- 150000002431 hydrogen Chemical class 0.000 claims description 21
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 21
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 17
- UQZPGHOJMQTOHB-UHFFFAOYSA-N 2-chloro-n-(2-chloroethyl)-n-ethylethanamine Chemical compound ClCCN(CC)CCCl UQZPGHOJMQTOHB-UHFFFAOYSA-N 0.000 claims description 16
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 15
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims description 15
- 125000004076 pyridyl group Chemical group 0.000 claims description 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 10
- 125000001153 fluoro group Chemical group F* 0.000 claims description 10
- 239000001301 oxygen Substances 0.000 claims description 10
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 10
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 8
- 125000000335 thiazolyl group Chemical group 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000002883 imidazolyl group Chemical group 0.000 claims description 6
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 6
- 125000006001 difluoroethyl group Chemical group 0.000 claims description 5
- VMJNTFXCTXAXTC-UHFFFAOYSA-N 2,2-difluoro-1,3-benzodioxole-5-carbonitrile Chemical group C1=C(C#N)C=C2OC(F)(F)OC2=C1 VMJNTFXCTXAXTC-UHFFFAOYSA-N 0.000 claims description 4
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000004857 imidazopyridinyl group Chemical group N1C(=NC2=C1C=CC=N2)* 0.000 claims description 4
- 125000001715 oxadiazolyl group Chemical group 0.000 claims description 4
- 125000002971 oxazolyl group Chemical group 0.000 claims description 4
- 125000001113 thiadiazolyl group Chemical group 0.000 claims description 4
- 125000001544 thienyl group Chemical group 0.000 claims description 4
- 125000001425 triazolyl group Chemical group 0.000 claims description 4
- PQIOSYKVBBWRRI-UHFFFAOYSA-N methylphosphonyl difluoride Chemical group CP(F)(F)=O PQIOSYKVBBWRRI-UHFFFAOYSA-N 0.000 claims description 3
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 2
- 125000004306 triazinyl group Chemical group 0.000 claims description 2
- 150000003254 radicals Chemical class 0.000 claims 45
- 150000001875 compounds Chemical class 0.000 claims 24
- 229910052736 halogen Inorganic materials 0.000 claims 24
- 150000002367 halogens Chemical class 0.000 claims 24
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 10
- 239000000203 mixture Substances 0.000 claims 9
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 8
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 8
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 7
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 7
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 6
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 5
- 241001465754 Metazoa Species 0.000 claims 5
- 241000607479 Yersinia pestis Species 0.000 claims 5
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 5
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 claims 5
- 238000009472 formulation Methods 0.000 claims 5
- 125000001072 heteroaryl group Chemical group 0.000 claims 5
- 125000005842 heteroatom Chemical group 0.000 claims 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 5
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 4
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims 4
- 125000004438 haloalkoxy group Chemical group 0.000 claims 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 claims 4
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 4
- 125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims 4
- XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical group OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 claims 4
- 239000003905 agrochemical Substances 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 3
- 125000000547 substituted alkyl group Chemical group 0.000 claims 3
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 3
- 125000005302 thiazolylmethyl group Chemical group [H]C1=C([H])N=C(S1)C([H])([H])* 0.000 claims 3
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims 3
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 2
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 claims 2
- 125000000069 2-butynyl group Chemical group [H]C([H])([H])C#CC([H])([H])* 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 125000004966 cyanoalkyl group Chemical group 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000004850 cyclobutylmethyl group Chemical group C1(CCC1)C* 0.000 claims 2
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 claims 2
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims 2
- 125000001188 haloalkyl group Chemical group 0.000 claims 2
- 125000005394 methallyl group Chemical group 0.000 claims 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 239000011593 sulfur Chemical group 0.000 claims 2
- 239000004094 surface-active agent Substances 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 claims 1
- HNEGJTWNOOWEMH-UHFFFAOYSA-N 1-fluoropropane Chemical group [CH2]CCF HNEGJTWNOOWEMH-UHFFFAOYSA-N 0.000 claims 1
- 125000006508 2,6-difluorobenzyl group Chemical group [H]C1=C([H])C(F)=C(C(F)=C1[H])C([H])([H])* 0.000 claims 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 1
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000006512 3,4-dichlorobenzyl group Chemical group [H]C1=C(Cl)C(Cl)=C([H])C(=C1[H])C([H])([H])* 0.000 claims 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 1
- 239000004606 Fillers/Extenders Substances 0.000 claims 1
- 241000282412 Homo Species 0.000 claims 1
- 239000004067 bulking agent Substances 0.000 claims 1
- 125000002944 cyanoaryl group Chemical group 0.000 claims 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004372 methylthioethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])* 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000005244 neohexyl group Chemical group [H]C([H])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 210000000056 organ Anatomy 0.000 claims 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 claims 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 1
- 230000000361 pesticidal effect Effects 0.000 claims 1
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims 1
- 230000001850 reproductive effect Effects 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 1
- 125000004632 tetrahydrothiopyranyl group Chemical group S1C(CCCC1)* 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- 238000011282 treatment Methods 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15154252.9 | 2015-02-09 | ||
| EP15154252 | 2015-02-09 | ||
| PCT/EP2016/052445 WO2016128298A1 (de) | 2015-02-09 | 2016-02-05 | Substituierte 2-thioimidazolyl-carboxamide als schädlingsbekämpfungsmittel |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018505887A JP2018505887A (ja) | 2018-03-01 |
| JP2018505887A5 true JP2018505887A5 (https=) | 2020-04-09 |
| JP6725522B2 JP6725522B2 (ja) | 2020-07-22 |
Family
ID=52462202
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017541623A Expired - Fee Related JP6725522B2 (ja) | 2015-02-09 | 2016-02-05 | 有害生物防除剤としての置換されている２−チオイミダゾリル−カルボキサミド類 |
Country Status (23)
| Country | Link |
|---|---|
| US (2) | US10368545B2 (https=) |
| EP (1) | EP3256462B1 (https=) |
| JP (1) | JP6725522B2 (https=) |
| KR (1) | KR20170115052A (https=) |
| CN (1) | CN107428732B (https=) |
| AR (1) | AR103637A1 (https=) |
| AU (1) | AU2016218054B2 (https=) |
| BR (1) | BR112017017122A2 (https=) |
| CA (1) | CA2975944A1 (https=) |
| CL (1) | CL2017002037A1 (https=) |
| CO (1) | CO2017008040A2 (https=) |
| DK (1) | DK3256462T3 (https=) |
| ES (1) | ES2752250T3 (https=) |
| IL (1) | IL253741B (https=) |
| MX (1) | MX374521B (https=) |
| PH (1) | PH12017501409A1 (https=) |
| PL (1) | PL3256462T3 (https=) |
| PT (1) | PT3256462T (https=) |
| RU (1) | RU2017131549A (https=) |
| TW (1) | TWI702212B (https=) |
| UY (1) | UY36551A (https=) |
| WO (1) | WO2016128298A1 (https=) |
| ZA (1) | ZA201706124B (https=) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108713017A (zh) * | 2016-02-11 | 2018-10-26 | 拜耳作物科学股份公司 | 用作害虫防治剂的取代的氧基咪唑基羧酰胺 |
| US10501441B2 (en) * | 2016-02-11 | 2019-12-10 | Bayer Cropscience Aktiengesellschaft | Substituted imidazolylcarboxamides as pesticides |
| US10544124B2 (en) * | 2016-02-11 | 2020-01-28 | Bayer Cropscience Aktiengesellschaft | Substituted 2-(het)arylimidazolylcarboxyamides as pesticides |
| ES2845902T3 (es) * | 2016-02-11 | 2021-07-28 | Bayer Cropscience Ag | 2-Oximidazolil-carboxamidas sustituidas como pesticidas |
| KR20190037305A (ko) | 2016-08-10 | 2019-04-05 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 해충 방제제로서의 치환된 2-헤테로시클릴 이미다졸릴-카르복스아미드 |
| EP3625219A1 (de) | 2017-05-15 | 2020-03-25 | Bayer Aktiengesellschaft | Verfahren zur herstellung von substituierten imidazolylcarboxyamiden |
| WO2019137995A1 (en) | 2018-01-11 | 2019-07-18 | Basf Se | Novel pyridazine compounds for controlling invertebrate pests |
| EP3725788A1 (en) | 2019-04-15 | 2020-10-21 | Bayer AG | Novel heteroaryl-substituted aminoalkyl azole compounds as pesticides |
| PL3962268T3 (pl) | 2019-05-03 | 2025-12-01 | Basf Se | Stabilizacja koncentratów w postaci stężonej zawiesiny z użyciem lignosulfonianu |
| WO2020224943A1 (en) | 2019-05-03 | 2020-11-12 | Basf Se | Stabilization of suspension concentrates by hydrophobic fumed silica |
| HUE073273T2 (hu) | 2019-05-03 | 2026-01-28 | Basf Se | Szuszpenziókoncentrátumok stabilizálása etoxilált ricinoleinnel |
| US20220274947A1 (en) * | 2019-07-23 | 2022-09-01 | Bayer Aktiengesellschaft | Novel heteroaryl-triazole compounds as pesticides |
| US12528798B2 (en) | 2019-10-29 | 2026-01-20 | Lg Chem, Ltd. | Compound for crop protectant |
| CN116046941B (zh) * | 2022-12-30 | 2024-06-25 | 徐州博康信息化学品有限公司 | 一种光刻胶树脂中残余单体含量的测试方法 |
| CN116751198B (zh) * | 2023-05-15 | 2026-04-14 | 上海工程技术大学 | 含异硫脲片段的咪唑并六元氮杂化合物的制备方法 |
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| SU725566A3 (ru) * | 1975-02-28 | 1980-03-30 | Плантекс Лтд (Фирма) | Способ получени производных имидазо/2,1-в/тиазолов или их кислотно- аддитивных или четвертичных аммонийных солей |
| DE2904548A1 (de) | 1979-02-07 | 1980-08-28 | Ruetgerswerke Ag | Verfahren zur herstellung von bis-2-pyridyl-disulfiden |
| DE3537290A1 (de) | 1985-10-19 | 1987-04-23 | Hoechst Ag | 1,2,5-substituierte imidazolverbindungen, verfahren zu ihrer herstellung und ihre verwendung als wachstumsregulatoren |
| DE3729852A1 (de) | 1987-09-05 | 1989-03-23 | Basf Ag | Verfahren zur herstellung von 1-alkylimidazol-5-carbonsaeuren sowie deren estern, amiden und nitrilen |
| US5002961A (en) * | 1987-10-19 | 1991-03-26 | Merrell Dow Pharmaceuticals | Method for reducing injury with imidazol-2-thionecarboxamides |
| ZA887662B (en) * | 1987-10-19 | 1989-06-28 | Merrell Dow Pharma | Method for reducing reperfusion injury with imidazol-2-thione-carboxamides |
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| GB0213715D0 (en) | 2002-06-14 | 2002-07-24 | Syngenta Ltd | Chemical compounds |
| TWI312272B (en) | 2003-05-12 | 2009-07-21 | Sumitomo Chemical Co | Pyrimidine compound and pests controlling composition containing the same |
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| GB0414438D0 (en) | 2004-06-28 | 2004-07-28 | Syngenta Participations Ag | Chemical compounds |
| WO2006043635A1 (ja) | 2004-10-20 | 2006-04-27 | Kumiai Chemical Industry Co., Ltd. | ３－トリアゾリルフェニルスルフィド誘導体及びそれを有効成分として含有する殺虫・殺ダニ・殺線虫剤 |
| WO2008134969A1 (fr) | 2007-04-30 | 2008-11-13 | Sinochem Corporation | Composés benzamides et leurs applications |
| GB0720126D0 (en) | 2007-10-15 | 2007-11-28 | Syngenta Participations Ag | Chemical compounds |
| TWI411395B (zh) | 2007-12-24 | 2013-10-11 | Syngenta Participations Ag | 殺蟲化合物 |
| TWI468407B (zh) | 2008-02-06 | 2015-01-11 | Du Pont | 中離子農藥 |
| CN101337940B (zh) | 2008-08-12 | 2012-05-02 | 国家农药创制工程技术研究中心 | 具杀虫活性的含氮杂环二氯烯丙醚类化合物 |
| EP2184273A1 (de) | 2008-11-05 | 2010-05-12 | Bayer CropScience AG | Halogen-substituierte Verbindungen als Pestizide |
| EP2409976A4 (en) | 2009-03-19 | 2012-09-19 | Taisho Pharmaceutical Co Ltd | GLYCINE TRANSPORTER INHIBITOR |
| EP2236505A1 (de) * | 2009-04-03 | 2010-10-06 | Bayer CropScience AG | Acylierte Aminopyridine und - pyridazine als Insektizide |
| WO2011009804A2 (en) * | 2009-07-24 | 2011-01-27 | Basf Se | Pyridine derivatives compounds for controlling invertebrate pests |
| WO2011093352A1 (ja) | 2010-01-27 | 2011-08-04 | 武田薬品工業株式会社 | チアゾール誘導体 |
| AR083431A1 (es) | 2010-06-28 | 2013-02-27 | Bayer Cropscience Ag | Compuestos heterociclicos como pesticidas |
| AU2011297160B2 (en) | 2010-08-31 | 2014-11-20 | Mitsui Chemicals Crop & Life Solutions, Inc. | Noxious organism control agent |
| AU2011347752A1 (en) | 2010-12-20 | 2013-07-11 | Basf Se | Pesticidal active mixtures comprising pyrazole compounds |
| CN102060818B (zh) | 2011-01-07 | 2012-02-01 | 青岛科技大学 | 一种新型螺螨酯类化合物及其制法与用途 |
| CN102057925B (zh) | 2011-01-21 | 2013-04-10 | 陕西上格之路生物科学有限公司 | 一种含噻虫酰胺和生物源类杀虫剂的杀虫组合物 |
| EP2830421B1 (en) | 2012-03-30 | 2017-03-01 | Basf Se | N-substituted pyridinylidene thiocarbonyl compounds and their use for combating animal pests |
| WO2014063942A1 (en) * | 2012-10-23 | 2014-05-01 | Basf Se | Substituted pesticidal pyrazole compounds |
-
2016
- 2016-02-04 TW TW105103675A patent/TWI702212B/zh not_active IP Right Cessation
- 2016-02-05 CN CN201680020375.1A patent/CN107428732B/zh not_active Expired - Fee Related
- 2016-02-05 US US15/546,234 patent/US10368545B2/en not_active Expired - Fee Related
- 2016-02-05 RU RU2017131549A patent/RU2017131549A/ru not_active Application Discontinuation
- 2016-02-05 AU AU2016218054A patent/AU2016218054B2/en not_active Ceased
- 2016-02-05 MX MX2017010293A patent/MX374521B/es active IP Right Grant
- 2016-02-05 KR KR1020177021761A patent/KR20170115052A/ko not_active Withdrawn
- 2016-02-05 WO PCT/EP2016/052445 patent/WO2016128298A1/de not_active Ceased
- 2016-02-05 PL PL16702955T patent/PL3256462T3/pl unknown
- 2016-02-05 PT PT167029552T patent/PT3256462T/pt unknown
- 2016-02-05 JP JP2017541623A patent/JP6725522B2/ja not_active Expired - Fee Related
- 2016-02-05 EP EP16702955.2A patent/EP3256462B1/de active Active
- 2016-02-05 AR ARP160100346A patent/AR103637A1/es unknown
- 2016-02-05 BR BR112017017122-8A patent/BR112017017122A2/pt not_active Application Discontinuation
- 2016-02-05 UY UY0001036551A patent/UY36551A/es unknown
- 2016-02-05 ES ES16702955T patent/ES2752250T3/es active Active
- 2016-02-05 CA CA2975944A patent/CA2975944A1/en not_active Abandoned
- 2016-02-05 DK DK16702955T patent/DK3256462T3/da active
-
2017
- 2017-07-31 IL IL253741A patent/IL253741B/en not_active IP Right Cessation
- 2017-08-07 PH PH12017501409A patent/PH12017501409A1/en unknown
- 2017-08-09 CO CONC2017/0008040A patent/CO2017008040A2/es unknown
- 2017-08-09 CL CL2017002037A patent/CL2017002037A1/es unknown
- 2017-09-08 ZA ZA2017/06124A patent/ZA201706124B/en unknown
-
2019
- 2019-06-13 US US16/439,911 patent/US20190307126A1/en not_active Abandoned
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