PT67090A

PT67090A - Process for the preparation of compounds for pest control

Process for the preparation of compounds for pest control

Info

Publication number: PT67090A
Authority: PT; Portugal
Prior art keywords: compounds; preparation; isopropenyl; formula; control
Prior art date: 1976-10-01

Application number

PT6709077A

Other languages

English (en)

Other versions

PT67090B (en

Original Assignee

American Cyanamid Co

Priority date

1976-10-01

Filing date

1977-09-28

Publication date

1977-10-01

1977-09-28 Application filed by American Cyanamid Co filed Critical American Cyanamid Co

1977-10-01 Publication of PT67090A publication Critical patent/PT67090A/pt

1978-03-20 Priority claimed from US05/890,568 external-priority patent/US4199595A/en

1980-08-18 Publication of PT67090B publication Critical patent/PT67090B/pt

Links

241000607479 Yersinia pestis Species 0.000 title 1
150000001875 compounds Chemical class 0.000 title 1
125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 abstract 2
241000238876 Acari Species 0.000 abstract 1
241000255925 Diptera Species 0.000 abstract 1
241000256244 Heliothis virescens Species 0.000 abstract 1
241000238631 Hexapoda Species 0.000 abstract 1
-1 Phenoxybenzyl esters Chemical class 0.000 abstract 1
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 abstract 1
239000002253 acid Substances 0.000 abstract 1
150000007513 acids Chemical class 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
239000003814 drug Substances 0.000 abstract 1
230000000694 effects Effects 0.000 abstract 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 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
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
230000003287 optical effect Effects 0.000 abstract 1
HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 abstract 1
229940070846 pyrethrins Drugs 0.000 abstract 1
239000002728 pyrethroid Substances 0.000 abstract 1
230000009885 systemic effect Effects 0.000 abstract 1