| Weight | 164.248 g/mol |
|---|---|
| Formula | C11H16O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
488-10-8 (6261-18-3, 488-10-8)
jasmone · cis-jasmone · (Z)-3-methyl-2-(2-pentenyl)-2-cyclopenten-1-one
Score:
#873 in Biochemistry
,
#2902 in Chemistry
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- New roles for cis jasmone as an insect semiochemical and in plant defense (Proceedings of the National Academy of Sciences of the United States of America, 2000)
- cis-Jasmone induces Arabidopsis genes that affect the chemical ecology of multitrophic interactions with aphids and their parasitoids. (Proceedings of the National Academy of Sciences of the United States of America, 2008)
- New synthesis of cyclopentenones. Methyl jasmonate and jasmone (Journal of Organic Chemistry, 1971)
- cis-Jasmone treatment induces resistance in wheat plants against the grain aphid, Sitobion avenae (Fabricius) (Homoptera: Aphididae) (Pest Management Science, 2003)
- Mild procedure for transforming nitro groups into carbonyls. Application to the synthesis of cis-jasmone (Journal of the American Chemical Society, 1971)
- Biosynthesis of cis-Jasmone: a pathway for the inactivation and the disposal of the plant stress hormone jasmonic acid to the gas phase? (Helvetica Chimica Acta, 1997)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - jasmone
- cis-jasmone
- (Z)-3-methyl-2-(2-pentenyl)-2-cyclopenten-1-one
- (Z)-jasmone
-
SMILESCCC=CCC1=C(CCC1=O)C
-
InChIKeyXMLSXPIVAXONDL-UHFFFAOYSA-N
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