SU291393A1 - - Google Patents
Info
- Publication number
- SU291393A1 SU291393A1 SU1305320A SU1305320A SU291393A1 SU 291393 A1 SU291393 A1 SU 291393A1 SU 1305320 A SU1305320 A SU 1305320A SU 1305320 A SU1305320 A SU 1305320A SU 291393 A1 SU291393 A1 SU 291393A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- cyclopropanecarboxylic acid
- pyrethrins
- pyrethrum
- allethrin
- synthesis
- Prior art date
Links
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 3
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 2
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 2
- 240000004460 Tanacetum coccineum Species 0.000 description 2
- VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 description 2
- ROVGZAWFACYCSP-MQBLHHJJSA-N [2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 description 2
- 229940024113 allethrin Drugs 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- -1 cyclopropanecarboxylic acid ester Chemical class 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 229940015367 pyrethrum Drugs 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- ZBJJDYGJCNTNTH-UHFFFAOYSA-N Betahistine mesilate Chemical group CS(O)(=O)=O.CS(O)(=O)=O.CNCCC1=CC=CC=N1 ZBJJDYGJCNTNTH-UHFFFAOYSA-N 0.000 description 1
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 244000042664 Matricaria chamomilla Species 0.000 description 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000004970 halomethyl group Chemical group 0.000 description 1
- 231100000086 high toxicity Toxicity 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
- 229940070846 pyrethrins Drugs 0.000 description 1
- 239000002728 pyrethroid Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU291393A1 true SU291393A1 (enrdf_load_stackoverflow) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3513241A (en) | Fungicidal and fungistatic n-(dialkylaminoalkyl) - carbamic acid and thiocarbamic acid esters | |
| US3835176A (en) | Alpha-cyanobenzyl cyclopropanecarboxylates | |
| US3792079A (en) | Benzyl chrysanthemumates | |
| EP0460575A1 (de) | Aromatische Verbindungen | |
| CA1061351A (en) | Cyclopropanecarboxylates | |
| HU184524B (en) | Insecticide and miticide compositions containing substituted acetate compounds as active agents, and process for producing the active agents | |
| HK1005721B (zh) | 香料的化合物 | |
| DE2436178B2 (de) | Cyclopropancarbonsaeureester, verfahren zu ihrer herstellung und ihre verwendung als pestizide | |
| JPH02233644A (ja) | 新規の２，２―ジメチル―３―（２―モノハロエテニル）シクロプロパンカルボン酸誘導体、それらの製造方法及び害虫駆除剤としてのそれらの使用 | |
| FI61478C (fi) | Vaextfungicida n-(1'-metoxi- och etoxikarbonyl-etyl)-n-acyl-anilinderivat | |
| SU291393A1 (enrdf_load_stackoverflow) | ||
| US3835220A (en) | Insecticidal composition comprising vinylcyclopropanecarboxylates | |
| FR2658819A1 (fr) | Nouveaux esters derives d'acide 3-(2-cyano 2-halogeno ethenyl) 2,2-dimethyl cyclopropanecarboxylique, leur procede de preparation et leur application comme pesticides. | |
| US3338783A (en) | Synergistic insecticidal compositions | |
| FR2568749A1 (fr) | Composition a base d'un derive de thiolcarbamate, procede pour prolonger l'action des herbicides et compositions herbicides ayant une action prolongee | |
| CH626042A5 (enrdf_load_stackoverflow) | ||
| US2350324A (en) | Parasiticidal composition | |
| CH639534A5 (de) | Fungizides mittel. | |
| KR880006161A (ko) | 3위치에 포함된 할로겐화 사슬을 갖는 2,2-디메틸시클로프로판 카르복실산의 신규유도체, 이들을 제조하기 위한 방법 및 중간체, 살충제로서 이들의 용도 및 이들을 함유하는 조성물 | |
| US2486579A (en) | Sulfoxide and sulfone compounds | |
| US3795740A (en) | Methylene dioxy benzene derivatives as synergists for carbaryl | |
| EP0521779B1 (fr) | Nouveaux esters pyréthrinoides de l'alcool 4-amino 2,3,5,6-tétrafluorophényl méthylique, leur procédé de préparation et leur application comme pesticides | |
| FR2687666A1 (fr) | Nouveaux esters pyrethrinouiques, derives de l'alcool 6-(trifluoromethyl) benzylique, leur procede de preparation et leur application comme pesticides. | |
| FR2678611A1 (fr) | Nouveaux esters pyrethrinouides de l'alcool 1,3,4,5,6,7-hexahydro 1,3-dioxo-2h-isoindol-2-yl-methylique, leur procede de preparation et leur application comme pesticides. | |
| FR2536748A1 (fr) | Nouveaux esters derives d'acides 2,2-dimethyl cyclopropane carboxyliques et d'alcools biaryliques, leur procede de preparation et leur application a la lutte contre les parasites |