AR106735A1 - Composiciones y métodos insecticidas - Google Patents
Composiciones y métodos insecticidasInfo
- Publication number
- AR106735A1 AR106735A1 ARP160103521A ARP160103521A AR106735A1 AR 106735 A1 AR106735 A1 AR 106735A1 AR P160103521 A ARP160103521 A AR P160103521A AR P160103521 A ARP160103521 A AR P160103521A AR 106735 A1 AR106735 A1 AR 106735A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- group
- alkyl
- hydrogen
- imidazole
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 9
- 238000000034 method Methods 0.000 title abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 12
- 239000001257 hydrogen Substances 0.000 abstract 12
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 12
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- 150000001875 compounds Chemical class 0.000 abstract 7
- 150000003839 salts Chemical class 0.000 abstract 7
- 241000238631 Hexapoda Species 0.000 abstract 6
- 125000003545 alkoxy group Chemical group 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 6
- 239000002689 soil Substances 0.000 abstract 4
- 125000003107 substituted aryl group Chemical group 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 241000607479 Yersinia pestis Species 0.000 abstract 2
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 2
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 230000000855 fungicidal effect Effects 0.000 abstract 2
- 239000000417 fungicide Substances 0.000 abstract 2
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 230000002363 herbicidal effect Effects 0.000 abstract 2
- 239000004009 herbicide Substances 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 2
- 239000002917 insecticide Substances 0.000 abstract 2
- 244000005700 microbiome Species 0.000 abstract 2
- 239000005645 nematicide Substances 0.000 abstract 2
- 125000005017 substituted alkenyl group Chemical group 0.000 abstract 2
- 125000005415 substituted alkoxy group Chemical group 0.000 abstract 2
- 125000004426 substituted alkynyl group Chemical group 0.000 abstract 2
- 125000004001 thioalkyl group Chemical group 0.000 abstract 2
- -1 (4- (2- (3-fluorophenyl) ) -5-phenyl-1H-imidazol-4-yl) phenyl Chemical group 0.000 abstract 1
- CTWRMVAKUSJNBK-UHFFFAOYSA-N 2-(2,4-dimethoxyphenyl)-4,5-diphenyl-1h-imidazole Chemical compound COC1=CC(OC)=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 CTWRMVAKUSJNBK-UHFFFAOYSA-N 0.000 abstract 1
- SZLSXVLLULZEPG-UHFFFAOYSA-N 2-(2,6-dichlorophenyl)-5-(2,5-dimethylphenyl)-4-phenyl-1h-imidazole Chemical compound CC1=CC=C(C)C(C2=C(N=C(N2)C=2C(=CC=CC=2Cl)Cl)C=2C=CC=CC=2)=C1 SZLSXVLLULZEPG-UHFFFAOYSA-N 0.000 abstract 1
- WNFATDXVVULQFJ-UHFFFAOYSA-N 2-(2-chloro-6-fluorophenyl)-5-(2,5-dimethylphenyl)-4-phenyl-1h-imidazole Chemical compound CC1=CC=C(C)C(C2=C(N=C(N2)C=2C(=CC=CC=2F)Cl)C=2C=CC=CC=2)=C1 WNFATDXVVULQFJ-UHFFFAOYSA-N 0.000 abstract 1
- XCCJHWPREGFUJH-UHFFFAOYSA-N 2-(2-ethoxyphenyl)-4,5-diphenyl-1h-imidazole Chemical compound CCOC1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 XCCJHWPREGFUJH-UHFFFAOYSA-N 0.000 abstract 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 abstract 1
- PMDIRJAOXIHIDD-UHFFFAOYSA-N 3-(2-chlorophenyl)-1-methyl-n-[2-(oxolan-2-yl)ethyl]pyrazole-4-carboxamide Chemical compound C=1C=CC=C(Cl)C=1C1=NN(C)C=C1C(=O)NCCC1CCCO1 PMDIRJAOXIHIDD-UHFFFAOYSA-N 0.000 abstract 1
- MPPFYEPPAUTRSW-UHFFFAOYSA-N 3-(2-chlorophenyl)-n-(2-ethoxyethyl)-1-methylpyrazole-4-carboxamide Chemical compound CCOCCNC(=O)C1=CN(C)N=C1C1=CC=CC=C1Cl MPPFYEPPAUTRSW-UHFFFAOYSA-N 0.000 abstract 1
- SUKJNCASPBTQCP-UHFFFAOYSA-N 4,5-bis(4-methylphenyl)-2-(4-methylsulfanylphenyl)-1h-imidazole Chemical compound C1=CC(SC)=CC=C1C1=NC(C=2C=CC(C)=CC=2)=C(C=2C=CC(C)=CC=2)N1 SUKJNCASPBTQCP-UHFFFAOYSA-N 0.000 abstract 1
- WJKZHNBAEYLNFN-UHFFFAOYSA-N 4,5-diphenyl-2-(2,3,4-trimethoxyphenyl)-1h-imidazole Chemical compound COC1=C(OC)C(OC)=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 WJKZHNBAEYLNFN-UHFFFAOYSA-N 0.000 abstract 1
- WSJQOBNXSVDWLW-UHFFFAOYSA-N 4,5-diphenyl-2-(2,4,6-trimethylphenyl)-1h-imidazole Chemical compound CC1=CC(C)=CC(C)=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)N1 WSJQOBNXSVDWLW-UHFFFAOYSA-N 0.000 abstract 1
- YVGAHZIITNQIGM-UHFFFAOYSA-N 4-(3-chlorophenyl)-2-(2,4-dichlorophenyl)-5-phenyl-1h-imidazole Chemical compound ClC1=CC=CC(C2=C(NC(=N2)C=2C(=CC(Cl)=CC=2)Cl)C=2C=CC=CC=2)=C1 YVGAHZIITNQIGM-UHFFFAOYSA-N 0.000 abstract 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 abstract 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 abstract 1
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 abstract 1
- PSECHVGJFFWNTD-UHFFFAOYSA-N n-(2-methylcyclohexyl)-1-phenyl-3-thiophen-2-ylpyrazole-4-carboxamide Chemical compound CC1CCCCC1NC(=O)C1=CN(C=2C=CC=CC=2)N=C1C1=CC=CS1 PSECHVGJFFWNTD-UHFFFAOYSA-N 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
Classifications
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C07D233/58—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Abstract
Reivindicación 1: Un método para controlar pestes de insectos, el método comprende: administrarle a una planta, semilla, suelo o insecto, una composición que comprende un compuesto de fórmula (1), un tautómero de este o una sal de este, donde R¹, R² y R³ se seleccionan independientemente del grupo que consiste en hidrógeno, halógeno, alquilo, alcoxi, tioalquilo, alqueniloxi, alquiniloxi, haloalquilo y haloalcoxi; donde R⁴ y R⁵ se seleccionan independientemente del grupo que consiste en hidrógeno, halógeno, alquilo, alcoxi, alquenoxi y alquinoxi; donde al menos uno de R¹ - R⁵ no es hidrógeno; donde R⁶ y R⁷ se seleccionan independientemente del grupo que consiste en hidrógeno, halógeno y alquilo; donde R⁸ se selecciona del grupo que consiste en hidrógeno, alquilo y acilfenilo opcionalmente sustituido; y donde R⁹ se selecciona del grupo que consiste en hidrógeno y alquilo. Reivindicación 3: El método de la reivindicación 1, donde una cantidad eficaz de un compuesto seleccionado del grupo que consiste en 2-mesitil-4,5-difenil-1H-imidazol, 2-(2,6-diclorofenil)-4-(2,5-dimetilfenil)-5-fenil-1H-imidazol, 2-(2-cloro-6-fluorofenil)-4-(2,5-dimetilfenil)-5-fenil-1H-imidazol, 2-(2,4-dimetoxifenil)-4,5-difenil-1H-imidazol, 2-(2-etoxifenil)-4,5-difenil-1H-imidazol, 4,5-difenil-2-(2-(prop-2-in-1-iloxi)fenil)-1H-imidazol, 5-(3-clorofenil)-2-(2,4-diclorofenil)-4-fenil-1H-imidazol, 4,5-difenil-2-(2,3,4-trimetoxifenil)-1H-imidazol, 2-(4-(metiltio)fenil)-4,5-di-p-tolil-1H-imidazol, (4-fluorofenil)(4-(2-(3-fluorofenil)-5-fenil-1H-imidazol-4-il)fenil)metanona, un tautómero de estos y una sal de estos se administra a la planta, semilla, suelo o insecto. Reivindicación 6: Una semilla tratada preparada de acuerdo con el método de la reivindicación 4, la semilla tratada comprende el compuesto de fórmula (1), un tautómero de este o una sal de este. Reivindicación 7: Una composición de tratamiento que comprende un compuesto de fórmula (1), un tautómero de este o una sal de este, donde R¹, R² y R³ se seleccionan independientemente del grupo que consiste en hidrógeno, halógeno, alquilo, alcoxi, tioalquilo, alqueniloxi, alquiniloxi, haloalquilo y haloalcoxi; donde R⁴ y R⁵ se seleccionan independientemente del grupo que consiste en hidrógeno, halógeno, alquilo, alcoxi, alquenoxi y alquinoxi; donde al menos uno de R¹ - R⁵ no es hidrógeno; donde R⁶ y R⁷ se seleccionan independientemente del grupo que consiste en hidrógeno, halógeno y alquilo; donde R⁸ se selecciona del grupo que consiste en hidrógeno, alquilo y acilfenilo opcionalmente sustituido; y donde R⁹ se selecciona del grupo que consiste en hidrógeno y alquilo. Reivindicación 9: La composición de tratamiento de la reivindicación 7 o la reivindicación 8, que comprende adicionalmente un fungicida, un insecticida, un nematicida, un herbicida, un microorganismo o mezclas de estos. Reivindicación 10: Un método para controlar pestes de insectos, el método comprende: administrarle a una planta, semilla, suelo o insecto, una composición que comprende un compuesto de fórmula (2) o una sal de este, donde R¹⁰ se selecciona del grupo que consiste en arilo opcionalmente sustituido y alquilo opcionalmente sustituido; donde R¹¹ se selecciona del grupo que consiste en arilo opcionalmente sustituido y heteroarilo opcionalmente sustituido; donde R¹² se selecciona del grupo que consiste en alquilo opcionalmente sustituido, alquenilo opcionalmente sustituido, alquinilo opcionalmente sustituido, alcoxi opcionalmente sustituido, heterocicloalquilo opcionalmente sustituido y cicloalquilo totalmente saturado opcionalmente sustituido; y donde Z es alquilo C₁₋₆ o un enlace. Reivindicación 13: El método de la reivindicación 10, donde una cantidad eficaz de un compuesto seleccionado del grupo que consiste en N-alil-3-fenil-1-(p-tolil)-1H-pirazol-4-carboxamida, N-(2-metilciclohexil)-1-fenil-3-(tiofen-2-il)-1H-pirazol-4-carboxamida, 3-(2-clorofenil)-N-(2-etoxietil)-1-metil-1H-pirazol-4-carboxamida, 3-(2-clorofenil)-1-metil-N-(2-(tetrahidrofuran-2-il)etil)-1H-pirazol-4-carboxamida, 3-(2-clorofenil)-1-metil-N-(tetrahidro-2H-tiopiran-4-il)-1H-pirazol-4-carboxamida y una sal de estos se administra en la planta, semilla, suelo o insecto. Reivindicación 18: Una composición de tratamiento que comprende un compuesto de fórmula (2) o una sal de este, donde R¹⁰ se selecciona del grupo que consiste en arilo opcionalmente sustituido y alquilo opcionalmente sustituido; donde R¹¹ se selecciona del grupo que consiste en arilo opcionalmente sustituido y heteroarilo opcionalmente sustituido; donde R¹² se selecciona del grupo que consiste en alquilo opcionalmente sustituido, alquenilo opcionalmente sustituido, alquinilo opcionalmente sustituido, alcoxi opcionalmente sustituido, heterocicloalquilo opcionalmente sustituido y cicloalquilo totalmente saturado opcionalmente sustituido; y donde Z es alquilo C₁₋₆ o un enlace. Reivindicación 20: La composición de tratamiento de la reivindicación 18 o la reivindicación 19, que comprende adicionalmente un fungicida, un insecticida, un nematicida, un herbicida, un microorganismo o mezclas de estos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562256867P | 2015-11-18 | 2015-11-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR106735A1 true AR106735A1 (es) | 2018-02-14 |
Family
ID=58717697
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP160103521A AR106735A1 (es) | 2015-11-18 | 2016-11-17 | Composiciones y métodos insecticidas |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US10827755B2 (es) |
| EP (1) | EP3377486A4 (es) |
| CN (1) | CN108349953B (es) |
| AR (1) | AR106735A1 (es) |
| BR (1) | BR112018009906B1 (es) |
| CA (1) | CA3002451A1 (es) |
| MX (1) | MX2018005549A (es) |
| WO (1) | WO2017087218A1 (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2018005549A (es) * | 2015-11-18 | 2018-11-09 | Monsanto Technology Llc | Composiciones y metodos insecticidas. |
| CN110149929A (zh) * | 2019-07-01 | 2019-08-23 | 遂宁市安居区坤元种植专业合作社 | 一种桃子高产种植方法 |
| CN110357820A (zh) * | 2019-08-14 | 2019-10-22 | 南通大学 | 一种含1-甲基-3-取代苯基吡唑结构的吡唑肟醚化合物及其制备方法和用途 |
| CN110754484B (zh) * | 2019-09-27 | 2021-05-25 | 贵州省果树科学研究所 | 一种降低火龙果园内农药残留的桑白蚧治方法 |
| TW202300650A (zh) | 2021-03-26 | 2023-01-01 | 美商旗艦先鋒創新有限責任（Ｖｉｉ）公司 | 真核系統中環狀多核糖核苷酸的產生 |
| WO2022204466A1 (en) | 2021-03-26 | 2022-09-29 | Flagship Pioneering Innovations Vii, Llc | Production of circular polyribonucleotides in a prokaryotic system |
| AR125217A1 (es) | 2021-03-26 | 2023-06-28 | Flagship Pioneering Innovations Vii Llc | Producción de polirribonucleótidos circulares en un sistema procariota |
| WO2023077118A1 (en) | 2021-11-01 | 2023-05-04 | Flagship Pioneering Innovations Vii, Llc | Polynucleotides for modifying organisms |
| WO2023141540A2 (en) | 2022-01-20 | 2023-07-27 | Flagship Pioneering Innovations Vii, Llc | Polynucleotides for modifying organisms |
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| NL296772A (es) * | 1962-03-21 | |||
| US3212966A (en) * | 1963-03-07 | 1965-10-19 | Air Prod & Chem | 2, 4, 5-triphenyl- and 2-naphthyl imidazole as nematocides |
| US3707475A (en) * | 1970-11-16 | 1972-12-26 | Pfizer | Antiinflammatory imidazoles |
| JPH0742204B2 (ja) * | 1984-07-27 | 1995-05-10 | ユニバ−シテイ オブ イリノイ | 光動力的除草剤 |
| JP3052364B2 (ja) * | 1989-12-19 | 2000-06-12 | 栗田工業株式会社 | ホスト化合物及び包接化合物 |
| JPH09176614A (ja) * | 1995-12-25 | 1997-07-08 | Japan Carlit Co Ltd:The | 紫外線吸収剤 |
| MY138097A (en) * | 2000-03-22 | 2009-04-30 | Du Pont | Insecticidal anthranilamides |
| US6558880B1 (en) * | 2001-06-06 | 2003-05-06 | Eastman Kodak Company | Thermally developable imaging materials containing heat-bleachable antihalation composition |
| EP1467985A1 (en) | 2002-01-22 | 2004-10-20 | E.I. Du Pont De Nemours And Company | Diamide invertebrate pest control agents |
| US7754738B2 (en) * | 2002-06-13 | 2010-07-13 | E.I. Du Pont De Nemours And Company | Pyrazole and pyrrole carboxamide insecticides |
| US7884120B2 (en) * | 2002-08-19 | 2011-02-08 | Lorus Therapeutics Inc. | 2,4,5-trisubstituted imidazoles and their use as anti-microbial agents |
| BR0314497A (pt) * | 2002-10-04 | 2005-08-02 | Du Pont | Composto, método e composição para controle de praga invertebrada, composição spray, composição isca e dispositivo para controle de praga invertebrada |
| WO2007024833A1 (en) * | 2005-08-24 | 2007-03-01 | E. I. Du Pont De Nemours And Company | Anthranilamides for controlling invertebrate pests |
| US7592362B2 (en) * | 2006-01-19 | 2009-09-22 | Pfizer Limited | Substituted imidazoles |
| JP2008280342A (ja) * | 2007-04-13 | 2008-11-20 | Sumitomo Chemical Co Ltd | 有害生物防除組成物 |
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| CN102464592B (zh) * | 2010-11-03 | 2014-09-03 | 中国中化股份有限公司 | 酰基苄胺类化合物及其应用 |
| TW201321367A (zh) | 2011-10-25 | 2013-06-01 | Du Pont | 經１，３－二芳基取代之雜環殺蟲劑 |
| WO2013096479A1 (en) * | 2011-12-19 | 2013-06-27 | E. I. Du Pont De Nemours And Company | Anthranilic diamide/polymer propagule-coating compositions |
| CN103254133A (zh) * | 2012-02-20 | 2013-08-21 | 南京大学 | 二芳基吡唑苯胺类化合物的制备及其在结肠癌治疗中的应用 |
| EP2883869A1 (en) | 2012-08-10 | 2015-06-17 | Daicel Corporation | Crystals containing unsaturated carboxylic acid amide compound and method for producing same |
| EP2903439A1 (en) * | 2012-10-01 | 2015-08-12 | Basf Se | Method of controlling ryanodine-modulator insecticide resistant insects |
| EP2984083B1 (en) * | 2013-04-10 | 2017-01-25 | Syngenta Participations AG | Pesticidally active substituted pyridyl carboxamides |
| CA2926433A1 (en) * | 2013-10-22 | 2015-04-30 | Dow Agrosciences Llc | Pesticidal compositions and related methods |
| CN104945326B (zh) * | 2015-06-24 | 2017-03-01 | 安徽农业大学 | 一种双吡唑酰胺类衍生物及其制备方法及在防治小菜蛾中的应用 |
| MX2018005549A (es) * | 2015-11-18 | 2018-11-09 | Monsanto Technology Llc | Composiciones y metodos insecticidas. |
-
2016
- 2016-11-09 MX MX2018005549A patent/MX2018005549A/es unknown
- 2016-11-09 CA CA3002451A patent/CA3002451A1/en active Pending
- 2016-11-09 US US15/777,124 patent/US10827755B2/en active Active
- 2016-11-09 BR BR112018009906-6A patent/BR112018009906B1/pt active IP Right Grant
- 2016-11-09 EP EP16866863.0A patent/EP3377486A4/en active Pending
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- 2016-11-09 WO PCT/US2016/061033 patent/WO2017087218A1/en active Application Filing
- 2016-11-17 AR ARP160103521A patent/AR106735A1/es unknown
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| Publication number | Publication date |
|---|---|
| US20180325112A1 (en) | 2018-11-15 |
| US11771088B2 (en) | 2023-10-03 |
| BR112018009906A2 (pt) | 2018-11-13 |
| CA3002451A1 (en) | 2017-05-26 |
| EP3377486A1 (en) | 2018-09-26 |
| WO2017087218A1 (en) | 2017-05-26 |
| CN108349953A (zh) | 2018-07-31 |
| US20210030001A1 (en) | 2021-02-04 |
| EP3377486A4 (en) | 2019-09-04 |
| CN108349953B (zh) | 2022-06-17 |
| BR112018009906B1 (pt) | 2022-05-31 |
| MX2018005549A (es) | 2018-11-09 |
| US10827755B2 (en) | 2020-11-10 |
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