| Approval: | AFNOR |
|---|---|
| IUPAC PIN: | (1S)-2-methyl-4-oxo-3-(prop-2-en-1-yl)cyclopent-2-en-1-yl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropane-1-carboxylate |
| IUPAC name: | (S)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate Rothamsted-style stereodescriptors: (S)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (1R)-trans-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate |
| CAS name: | (1S)-2-methyl-4-oxo-3-(2-propen-1-yl)-2-cyclopenten-1-yl (1R,3R)-2,2-dimethyl-3-(2-methyl-1-propen-1-yl)cyclopropanecarboxylate |
| CAS Reg. No.: | 28434-00-6 |
| Formula: | C19H26O3 |
| Activity: | insecticides (pyrethroid) |
| Notes: | There is no ISO common name for this substance; the name “esdépalléthrine” is approved by the Association Française de Normalisation. The name “S-bioallethrin” (S-生物烯丙菊酯) is approved in China. The unresolved mixture of stereoisomers has the ISO common name allethrin [584-79-2], and one partially resolved mixture of stereoisomers has the ISO common name bioallethrin [260359-57-7]. |
| Structure: |  |
| Pronunciation: | |
| InChIKey: | ZCVAOQKBXKSDMS-PVAVHDDUSA-N |
| InChI: | InChI=1S/C19H26O3/c1-7-8-13-12(4)16(10-15(13)20)22-18(21)17-14(9-11(2)3)19(17,5)6/h7,9,14,16-17H,1,8,10H2,2-6H3/t14-,16+,17+/m1/s1 |