| Approval: | ISO |
|---|---|
| IUPAC PIN: | (1Ξ)-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: | (1RS)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate Rothamsted-style stereodescriptors: (1RS)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (1R)-trans-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate pre-1969 name: (±)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (+)-trans-chrysanthemate |
| CAS name: | 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.: | 260359-57-7 |
| Formula: | C19H26O3 |
| Activity: | insecticides (pyrethroid) |
| Notes: | The name “d-trans-allethrin” is approved by the Entomological Society of America, and is also approved in China (右旋反式烯丙菊酯). * The name “dépalléthrine” (n.f.) is approved by the Association Française de Normalisation. The unresolved mixture of stereoisomers has the ISO common name allethrin [584-79-2]. The (S)-alcohol stereoisomer has the AFNOR common name esdépalléthrine [28434-00-6]. |
| Structure: |  |
| Pronunciation: | bī-ō-ǎl-lēth-rǐn Guide to British pronunciation |
| InChIKey: | ZCVAOQKBXKSDMS-AQYZNVCMSA-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 |