AR086587A1 - Compuestos insecticidas - Google Patents
Compuestos insecticidasInfo
- Publication number
- AR086587A1 AR086587A1 ARP120101879A ARP120101879A AR086587A1 AR 086587 A1 AR086587 A1 AR 086587A1 AR P120101879 A ARP120101879 A AR P120101879A AR P120101879 A ARP120101879 A AR P120101879A AR 086587 A1 AR086587 A1 AR 086587A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- substituted
- haloalkyl
- alkoxy
- cycloalkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 239000002917 insecticide Substances 0.000 title 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 13
- 125000006648 (C1-C8) haloalkyl group Chemical group 0.000 abstract 8
- 125000003545 alkoxy group Chemical group 0.000 abstract 8
- 229910052717 sulfur Inorganic materials 0.000 abstract 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 5
- -1 carbonyl- Chemical group 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical group 0.000 abstract 4
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 3
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 2
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 abstract 1
- 241000238631 Hexapoda Species 0.000 abstract 1
- 241000237852 Mollusca Species 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 241000244206 Nematoda Species 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- 230000000895 acaricidal effect Effects 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000001246 bromo group Chemical group Br* 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- 125000004850 cyclobutylmethyl group Chemical group C1(CCC1)C* 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000006001 difluoroethyl group Chemical group 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 230000000749 insecticidal effect Effects 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000002013 molluscicidal effect Effects 0.000 abstract 1
- 230000001069 nematicidal effect Effects 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000003566 oxetanyl group Chemical group 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000011593 sulfur Substances 0.000 abstract 1
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D327/00—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
- C07D327/02—Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms one oxygen atom and one sulfur atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D411/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D411/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D411/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Tropical Medicine & Parasitology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Procesos e intermedios para preparar estos compuestos, a composiciones insecticidas acaricidas, nematicidas y molusquicidas que comprenden estos compuestos y a métodos para emplear estos compuestos con el fin de controlar plagas de insectos, acáridos, nematodos y moluscos.Reivindicación 1: Un compuesto de fórmula (1), donde A1, A2, A3 y A4 son, independientemente unos de otros, C-H, C-R5 o nitrógeno; B1--B2--B3-B4 es -CH2-C=N-CH2-, -CH2-N-CH2-CH2-, -CH2-C=CH-O-o -CH=C-CH2-O-; G1 es oxígeno o azufre; L es un enlace sencillo o alquileno C1-8; R1 es hidrógeno, alquilo C1-8, (alquil C1-8)carbonil-, alcoxi C1-8, (alcoxi C1-8)-(alquilo C1-8), alquenilo C2-8, alquinilo C2-8, arilo o arilo sustituido con de uno a tres R6, o R1 es heterociclilo o heterociclilo sustituido con de uno a tres R6 o (alcoxi C1-8)carbonil-; R2 es hidrógeno, haloalquilo C1-8 o alquilo C1-8; R3 es haloalquilo C1-8; R4 es arilo o arilo sustituido con uno a tres R6, o R4 es heterociclilo o heterociclilo sustituido con de uno a tres R6; cada R5 es independiente halógeno, ciano, nitro, alquilo C1-8, cicloalquilo C3-8, haloalquilo C1-8, alquenilo C2-8, haloalquenilo C2-8, alquinilo C2-8, haloalquinilo C2-8, alcoxi C1-8, haloalcoxi C1-8, (alcoxi C1-8)carbonil-, o dos R5 en átomos de carbono adyacentes juntos forman un puente -CH=CH-CH=CH- o un puente -N=CH-CH=CH-; cada R6 es independientemente halógeno, ciano, nitro, alquilo C1-8, haloalquilo C1-8, alcoxi C1-8 o haloalcoxi C1-8; Y1 es CR7R8, C=O o C=S; Y2, Y3 e Y4 son independientemente CR7R8, C=O, C=S, N-R9, O, S, SO ó SO2; donde al menos dos átomos del anillo adyacentes en el anillo formado por Y1, Y2, Y3 e Y4 son heteroátomos; cada R7 y R8 es independientemente hidrogeno, halógeno, alquilo C1-8 o haloalquilo C1-8; cada R9 es independientemente hidrógeno, ciano, ciano-(alquilo C1-8), alquilo C1-8, haloalquilo C1-8, cicloalquilo C3-8, cicloalquilo C3-8 donde un átomo de carbono se reemplaza por O, S, S(O) ó SO2, o (cicloalquil C3-8)-(alquilo C1-8), (cicloalquil C3-8)-(alquilo C1-8) donde un átomo de carbono en el grupo cicloalquilo se reemplaza por O, S, S(O) ó SO2, o (cicloalquil C3-8)-(haloalquilo C1-8), hidroxialquilo C1-8, (alcoxi C1-8)-(alquilo C1-8), alquenilo C2-8, haloalquenilo C2-8, alquinilo C2-8 haloalquinilo C1-8, fenilo, fenilo sustituido con de uno a tres R10, heteroarilo, heteroarilo sustituido con de uno a tres R10, fenil-(alquilo C1-4), fenil-(alquilo C1-4) donde el resto fenilo está sustituido con de uno a tres R10, heteroaril-(alquilo C1-4) o heteroaril-(alquilo C1-4) donde el resto heroarilo está sustituido con de uno a tres R10, o (alquil C1-4)-(alquil C1-4-O-N=)C-CH2,-; cada R10 es independientemente halógeno, ciano, nitro, alquilo C1-8, haloalquilo C1-8, alcoxi C1-8 o haloalcoxi C1-8; o una de sus sales o N-óxidos; con la condición de que, cuando B1--B2--B3-B4 sea -CH2-C=CH-O- o -CH=C-CH,-O-, Y1-Y2-Y3-Y4 no sea CH2-O-N(Ra)C(=O)-, donde Ra es hidrógeno, metilo, etilo, propilo, isopropilo, butilo, ciclopropilo, ciclopropilmetilo, ciclobutilo, ciclobutilmetilo, oxetanilo, tietanilo, trifluoroetilo, difluoroetilo, alilo, propargilo, cianometilo, bencilo, bencilo sustituido con de uno a tres Rb, o Ra es piridilmetil- o piridilmetil- sustituido con de uno a tres Rb; y cada Rb es independientemente fluoro, cloro, bromo, trifluorometilo, trifluorometoxi ciano o metoxi.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11168217 | 2011-05-31 | ||
| EP11173293 | 2011-07-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR086587A1 true AR086587A1 (es) | 2014-01-08 |
Family
ID=46201626
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP120101879A AR086587A1 (es) | 2011-05-31 | 2012-05-29 | Compuestos insecticidas |
Country Status (11)
| Country | Link |
|---|---|
| US (3) | US9545106B2 (es) |
| EP (1) | EP2714666B1 (es) |
| JP (1) | JP5972971B2 (es) |
| KR (1) | KR20140042821A (es) |
| CN (2) | CN103562189B (es) |
| AR (1) | AR086587A1 (es) |
| BR (1) | BR112013030622A2 (es) |
| MX (1) | MX2013013857A (es) |
| TW (1) | TW201311677A (es) |
| UY (1) | UY34104A (es) |
| WO (1) | WO2012163959A1 (es) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW201311677A (zh) * | 2011-05-31 | 2013-03-16 | Syngenta Participations Ag | 殺蟲化合物 |
| US9487489B2 (en) | 2013-02-06 | 2016-11-08 | Bayer Cropscience Aktiengesellschaft | Halogen-substituted pyrazole derivatives as pest-control agents |
| EA030935B1 (ru) | 2013-11-01 | 2018-10-31 | Мериал, Инк. | Антипаразитарные и пестицидные изоксазолиновые соединения |
| JP6140373B2 (ja) * | 2013-11-18 | 2017-05-31 | ノバルティス ティーアゲズントハイト アーゲー | 新規化合物 |
| MX2016008653A (es) | 2014-01-03 | 2016-09-26 | Bayer Animal Health Gmbh | Nuevas pirazolil-heteroarilamidas como agentes plaguicidas. |
| PE20161068A1 (es) | 2014-02-26 | 2016-10-21 | Basf Se | Compuestos de azolina |
| CN108822053A (zh) * | 2014-04-30 | 2018-11-16 | 先正达参股股份有限公司 | 用于制备取代的环丝氨酸的方法 |
| JP2017521441A (ja) | 2014-07-15 | 2017-08-03 | バイエル・アニマル・ヘルス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ａｎｉｍａｌ Ｈｅａｌｔｈ Ｇｍｂｈ | 有害生物防除剤としてのアリール−トリアゾリルピリジン類 |
| ES2860908T3 (es) | 2014-12-22 | 2021-10-05 | Basf Se | Compuestos de azolina sustituidos por un sistema de anillo condensado |
| ES2733532T3 (es) | 2014-12-22 | 2019-11-29 | Basf Se | Compuestos de azolina sustituidos por un sistema de anillo carbocíclico condensado |
| US20180072718A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyridine compounds and uses thereof |
| US20180072741A1 (en) | 2016-09-09 | 2018-03-15 | Incyte Corporation | Pyrazolopyrimidine compounds and uses thereof |
| MX389700B (es) | 2016-09-09 | 2025-03-20 | Incyte Corp | Derivados de pirazolopiridina como moduladores de cinasa 1 progenitora hematopoyetica (hpk1) y usos de los mismos para tratamiento de cancer. |
| US20180228786A1 (en) | 2017-02-15 | 2018-08-16 | Incyte Corporation | Pyrazolopyridine compounds and uses thereof |
| US11104671B2 (en) * | 2017-03-23 | 2021-08-31 | Syngenta Participations Ag | Insecticidal compounds |
| WO2019051199A1 (en) | 2017-09-08 | 2019-03-14 | Incyte Corporation | 6-CYANO-INDAZOLE COMPOUNDS AS HEMATOPOIETIC PROGENITOR KINASE 1 (HPK1) MODULATORS |
| CN112292380B (zh) | 2018-02-20 | 2024-04-05 | 因赛特公司 | 作为用于治疗癌症的hpk1抑制剂的n-(苯基)-2-(苯基)嘧啶-4-甲酰胺衍生物及相关化合物 |
| US10745388B2 (en) | 2018-02-20 | 2020-08-18 | Incyte Corporation | Indazole compounds and uses thereof |
| US10752635B2 (en) | 2018-02-20 | 2020-08-25 | Incyte Corporation | Indazole compounds and uses thereof |
| US11299473B2 (en) | 2018-04-13 | 2022-04-12 | Incyte Corporation | Benzimidazole and indole compounds and uses thereof |
| US10899755B2 (en) | 2018-08-08 | 2021-01-26 | Incyte Corporation | Benzothiazole compounds and uses thereof |
| US11111247B2 (en) | 2018-09-25 | 2021-09-07 | Incyte Corporation | Pyrazolopyrimidine compounds and uses thereof |
| EP3891113B1 (en) | 2018-12-04 | 2022-08-17 | Basf Se | Process for preparation of 5-bromo-1,3-dichloro-2-fluoro-benzene |
| EP4010338A1 (en) | 2019-08-06 | 2022-06-15 | Incyte Corporation | Solid forms of an hpk1 inhibitor |
| KR20230043904A (ko) | 2020-07-24 | 2023-03-31 | 엘랑코 유에스 인코포레이티드 | 이속사졸린 화합물 및 이의 중간체의 제조 공정 |
| WO2023039078A1 (en) * | 2021-09-08 | 2023-03-16 | Isca Technologies, Inc. | Methods and compositions for controlling tomato leaf miner |
| US20250049032A1 (en) * | 2021-12-17 | 2025-02-13 | Salk Institute For Biological Studies | Ethylene signaling activator modulates root system architecture |
| JP2025517548A (ja) | 2022-05-30 | 2025-06-05 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | ４－置換２－オキサゾリジノンの調製プロセス |
| CN118985621B (zh) * | 2024-08-27 | 2025-09-05 | 北农（海利）涿州种衣剂有限公司 | 含氟吡呋喃酮与异噁唑虫酰胺的杀虫组合物 |
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| CN104582487B (zh) * | 2012-08-24 | 2019-05-31 | 先正达参股股份有限公司 | 控制昆虫的方法 |
| ES2736314T3 (es) * | 2012-08-24 | 2019-12-27 | Syngenta Participations Ag | Métodos para controlar gusanos elatéridos |
-
2012
- 2012-05-29 TW TW101119093A patent/TW201311677A/zh unknown
- 2012-05-29 AR ARP120101879A patent/AR086587A1/es unknown
- 2012-05-29 UY UY0001034104A patent/UY34104A/es not_active Application Discontinuation
- 2012-05-30 CN CN201280026282.1A patent/CN103562189B/zh not_active Expired - Fee Related
- 2012-05-30 JP JP2014513172A patent/JP5972971B2/ja not_active Expired - Fee Related
- 2012-05-30 US US14/118,573 patent/US9545106B2/en not_active Expired - Fee Related
- 2012-05-30 CN CN201611059189.7A patent/CN106588904A/zh active Pending
- 2012-05-30 MX MX2013013857A patent/MX2013013857A/es not_active Application Discontinuation
- 2012-05-30 EP EP12724985.2A patent/EP2714666B1/en not_active Not-in-force
- 2012-05-30 KR KR1020137034059A patent/KR20140042821A/ko not_active Withdrawn
- 2012-05-30 BR BR112013030622A patent/BR112013030622A2/pt not_active Application Discontinuation
- 2012-05-30 WO PCT/EP2012/060125 patent/WO2012163959A1/en active Application Filing
-
2016
- 2016-11-28 US US15/361,838 patent/US9913471B2/en active Active
-
2018
- 2018-02-05 US US15/888,289 patent/US10869477B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP2714666B1 (en) | 2018-02-07 |
| CN106588904A (zh) | 2017-04-26 |
| CN103562189A (zh) | 2014-02-05 |
| US20140107056A1 (en) | 2014-04-17 |
| KR20140042821A (ko) | 2014-04-07 |
| US10869477B2 (en) | 2020-12-22 |
| TW201311677A (zh) | 2013-03-16 |
| US9545106B2 (en) | 2017-01-17 |
| JP5972971B2 (ja) | 2016-08-17 |
| CN103562189B (zh) | 2016-11-23 |
| BR112013030622A2 (pt) | 2016-08-16 |
| JP2014516978A (ja) | 2014-07-17 |
| WO2012163959A1 (en) | 2012-12-06 |
| US9913471B2 (en) | 2018-03-13 |
| MX2013013857A (es) | 2014-03-05 |
| US20170071207A1 (en) | 2017-03-16 |
| UY34104A (es) | 2013-01-03 |
| US20180153170A1 (en) | 2018-06-07 |
| EP2714666A1 (en) | 2014-04-09 |
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