RU93005172A - PESTICIDAL COMPOUND, INSECTICIDAL OR ACARICIDAL COMPOSITION, METHOD OF FIGHT AGAINST INSECTS OR ACARICIDES - Google Patents
PESTICIDAL COMPOUND, INSECTICIDAL OR ACARICIDAL COMPOSITION, METHOD OF FIGHT AGAINST INSECTS OR ACARICIDESInfo
- Publication number
- RU93005172A RU93005172A RU93005172/04A RU93005172A RU93005172A RU 93005172 A RU93005172 A RU 93005172A RU 93005172/04 A RU93005172/04 A RU 93005172/04A RU 93005172 A RU93005172 A RU 93005172A RU 93005172 A RU93005172 A RU 93005172A
- Authority
- RU
- Russia
- Prior art keywords
- alkyl
- acaricides
- insecticidal
- halogen
- hydrogen
- Prior art date
Links
- 241000238631 Hexapoda Species 0.000 title 1
- 230000000895 acaricidal Effects 0.000 title 1
- 239000000642 acaricide Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 230000000749 insecticidal Effects 0.000 title 1
- 230000000361 pesticidal Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000001188 haloalkyl group Chemical group 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- -1 phenylethynyl Chemical group 0.000 claims 3
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- JAABUGUCYZQMID-UHFFFAOYSA-N 2-ethyl-1-benzothiophene Chemical class C1=CC=C2SC(CC)=CC2=C1 JAABUGUCYZQMID-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 125000006598 aminocarbonylamino group Chemical group 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 125000000262 haloalkenyl group Chemical group 0.000 claims 1
- 125000005429 oxyalkyl group Chemical group 0.000 claims 1
- 239000000575 pesticide Substances 0.000 claims 1
- 125000004665 trialkylsilyl group Chemical group 0.000 claims 1
Claims (1)
в которой R выбирают из
R1 выбирают из водорода, галогена, низшего алкила, низшего галоадалкила и фенилэтинила, R2 выбирают из водорода, галогена, низшего алкила, низшей алкилтиогруппы, низшего галоидалкенила, галоидалкенилтио - группы, фенил низший алкенил группы, формила, низшего алкоксикарбонила, карбокси низший акленил группы, низший алкоксикарбонил низший алкенил группы, фенила, 2-тиенила, и метилтиен - 2-ила, R3 выбирают из алкила, низшего триалкилсилила, низшего галоидалкила, оксиалкила, алкилкарбонила, метилтиен-2-ила, 2-тиенила и бензотиен-2-ила, R4 выбирают из водорода, галогена, низшего алкила, низшего галоидалкила, низшей алкоксигруппы, низшей галоидалкилтиогруппы, низшего алкоксикарбонила, аминогруппы и алкилкарбониламиногруппы, R5 выбирают из водорода, низшего алкила и низшего галоидалкила.Ethylbenzothiophene compounds of the following formula are proposed, which act as pesticides:
in which R is chosen from
R 1 is selected from hydrogen, halogen, lower alkyl, lower galoadalkila and phenylethynyl, R 2 is selected from hydrogen, halogen, lower alkyl, lower alkylthio, lower haloalkenyl, galoidalkeniltio - group, a phenyl lower alkenyl group, formyl, lower alkoxycarbonyl, carboxy lower aklenil groups, lower alkoxycarbonyl lower alkenyl groups, phenyl, 2-thienyl, and methylthien-2-yl, R 3 is selected from alkyl, lower trialkylsilyl, lower haloalkyl, oxyalkyl, alkylcarbonyl, methylthien-2-yl, 2-thienyl and benzothien-2 phenylpropionate, R 4 is selected from odoroda, halogen, lower alkyl, lower haloalkyl, lower alkoxy, lower galoidalkiltiogruppy, lower alkoxycarbonyl, amino, and alkylcarbonylamino, R 5 is selected from hydrogen, lower alkyl and lower haloalkyl.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/549,516 US5073564A (en) | 1990-07-06 | 1990-07-06 | Ethynylbenzothiophene pesticides |
| US549.516 | 1990-07-06 | ||
| PCT/US1991/004739 WO1992000672A1 (en) | 1990-07-06 | 1991-07-03 | Ethynylbenzothiophene pesticides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU93005172A true RU93005172A (en) | 1995-09-20 |
| RU2079495C1 RU2079495C1 (en) | 1997-05-20 |
Family
ID=24193336
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU9193005172A RU2079495C1 (en) | 1990-07-06 | 1991-07-03 | Ethynylbenzothienyls |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5073564A (en) |
| EP (1) | EP0538310B1 (en) |
| AU (1) | AU641256B2 (en) |
| CA (1) | CA2083492A1 (en) |
| DE (1) | DE69113044T2 (en) |
| ES (1) | ES2078532T3 (en) |
| RU (1) | RU2079495C1 (en) |
| WO (1) | WO1992000672A1 (en) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5183827A (en) * | 1989-09-19 | 1993-02-02 | Allergan, Inc. | Acetylenes disubstituted with a heteroaromatic group and a 2-substituted chromanyl, thiochromanyl or 1,2,3,4-tetrahydroquinolinyl group having retinoid-like activity |
| US5272156A (en) * | 1989-09-19 | 1993-12-21 | Allergan, Inc. | Acetylenes disubstituted with a heteroaromatic group and a 2-substituted 1,2,3,4-tetrahydroquinolinyl group having retinoid-like activity |
| US5264456A (en) * | 1989-12-29 | 1993-11-23 | Allergan, Inc. | Acetylenes disubstituted with a furyl group and a substituted phenyl group having retinoid like activity |
| KR100902171B1 (en) * | 2001-03-08 | 2009-06-10 | 더 트러스티스 오브 더 유니버시티 오브 펜실베니아 | Facially amphiphilic polymers as anti-infective agents |
| EP2471524A3 (en) | 2003-03-17 | 2012-12-12 | The Trustees Of The University Of Pennsylvania | Facially amphiphllic polymers and oligomers and uses thereof |
| US8222456B2 (en) | 2004-01-23 | 2012-07-17 | The Trustees Of The University Of Pennsylvania | Facially amphiphilic polyaryl and polyarylalkynyl polymers and oligomers and uses thereof |
| AU2006218805A1 (en) * | 2005-02-25 | 2006-09-08 | The Trustees Of The University Of Pennsylvania | Facially amphiphilic polymers and oligomers, compositions thereof, and use thereof in methods of treating cancer |
| NZ601866A (en) * | 2007-06-29 | 2013-12-20 | Acucela Inc | Alkynyl phenyl derivative compounds for treating ophthalmic diseases and disorders |
| TWI708770B (en) * | 2015-06-08 | 2020-11-01 | 日商捷恩智股份有限公司 | Liquid crystal compound having benzothiophene, liquid crystal composition and liquid crystal display device |
| TWI694068B (en) * | 2015-10-13 | 2020-05-21 | 日商捷恩智股份有限公司 | Liquid crystal compound with benzothiophene, liquid crystal composition and liquid crystal display element |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4908357A (en) * | 1986-04-30 | 1990-03-13 | Fmc Corporation | Photoactive azole pesticides |
| US4826829A (en) * | 1986-07-23 | 1989-05-02 | Fmc Corporation | 2-Substituted ethynyl thiophene pesticides |
| US4788207A (en) * | 1988-02-29 | 1988-11-29 | Fmc Corporation | Photoactivated miticidal and insecticidal ethynylthiazoles |
| US4889867A (en) * | 1988-11-15 | 1989-12-26 | Fmc Corporation | Photoactivated miticidal and insecticidal ethynyl-thiazoles |
-
1990
- 1990-07-06 US US07/549,516 patent/US5073564A/en not_active Expired - Fee Related
-
1991
- 1991-07-03 EP EP91912491A patent/EP0538310B1/en not_active Expired - Lifetime
- 1991-07-03 RU RU9193005172A patent/RU2079495C1/en active
- 1991-07-03 DE DE69113044T patent/DE69113044T2/en not_active Expired - Fee Related
- 1991-07-03 AU AU81066/91A patent/AU641256B2/en not_active Ceased
- 1991-07-03 CA CA002083492A patent/CA2083492A1/en not_active Abandoned
- 1991-07-03 ES ES91912491T patent/ES2078532T3/en not_active Expired - Lifetime
- 1991-07-03 WO PCT/US1991/004739 patent/WO1992000672A1/en active IP Right Grant
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