CAS 4466-14-2: Jasmolin I
Formula:C21H30O3
InChI:InChI=1S/C21H30O3/c1-7-8-9-10-15-14(4)18(12-17(15)22)24-20(23)19-16(11-13(2)3)21(19,5)6/h8-9,11,16,18-19H,7,10,12H2,1-6H3/b9-8-/t16-,18+,19+/m1/s1
InChI key:InChIKey=NZKIRHFOLVYKFT-VUMXUWRFSA-N
SMILES:C(O[C@@H]1C(C)=C(C/C=C\CC)C(=O)C1)(=O)[C@@H]2[C@@H](C=C(C)C)C2(C)C
Synonyms:- (1R-(1alpha(S*(Z)),3beta))-2-Methyl-4-oxo-3-(2-pentenyl)-2-cyclopenten-1-yl 2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate
- (1S)-2-methyl-4-oxo-3-[(2Z)-pent-2-en-1-yl]cyclopent-2-en-1-yl (1R,3R)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate
- 2-methyl-4-oxo-3-[(2E)-pent-2-en-1-yl]cyclopent-2-en-1-yl 2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate
- Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propen-1-yl)-, (1S)-2-methyl-4-oxo-3-(2Z)-2-penten-1-yl-2-cyclopenten-1-yl ester, (1R,3R)-
- Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, (1S)-2-methyl-4-oxo-3-(2Z)-2-pentenyl-2-cyclopenten-1-yl ester, (1R,3R)-
- Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, 2-methyl-4-oxo-3-(2-pentenyl)-2-cyclopenten-1-yl ester, (1R-(1alpha(S*(Z)),3beta))-
- Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methyl-1-propenyl)-, 2-methyl-4-oxo-3-(2-pentenyl)-2-cyclopenten-1-yl ester, [1R-[1α[S*(Z)],3β]]-
- Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methylpropenyl)-, ester with 4-hydroxy-3-methyl-2-(2-pentenyl)-2-cyclopenten-1-one
- Jasmolin I
- Jasmoline I
- Jasmoline I [ISO-French]
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Found 3 products.
Jasmolin I
CAS:Jasmolin I is a botanical insecticide derived from the pyrethrum plant, Chrysanthemum cinerariifolium. It acts primarily through neurotoxic mechanisms, targeting the sodium channels in the nervous systems of insects. The interaction prolongs the open state of the sodium channels, resulting in repetitive discharges and ultimately paralysis of the target pests. Jasmolin I is utilized in various applications, including agriculture and household pest control, due to its effectiveness against a wide range of insect pests. Its natural origin makes it an appealing choice in integrated pest management programs, especially where minimal environmental impact is a priority. However, its relatively rapid degradation in sunlight necessitates careful timing of applications, and it is often used in conjunction with synergists to enhance its stability and efficacy.Formula:C21H30O3Purity:Min. 95%Molecular weight:330.46 g/mol
