cis-Jasmone (488-10-8)

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Suppliers

• Sigma-Aldrich - cis-Jasmone
  40.00 - 706.00 USD
• Fisher Scientific - Search for cis-Jasmone
• TCI - cis-Jasmone
  25.00 - 70.00 USD

Most-cited Publications

• 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)

Areas of Application

Safety

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Trends

Alternate Names

• jasmone
• (Z)-3-methyl-2-(2-pentenyl)-2-cyclopenten-1-one
• (Z)-jasmone
• SMILES
  CCC=CCC1=C(CCC1=O)C
• InChIKey
  XMLSXPIVAXONDL-UHFFFAOYSA-N

External Links

• Pubchem - cis-Jasmone
• Wikipedia - jasmone
  Jasmone is an organic compound, which is a volatile portion of the oil from jasmine flowers. It is a colorless to pale yellow liquid. Jasmone can exist in two isomeric forms with differing geometry around the pentenyl double bond, cis-jasmone and trans-jasmone.

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cis-Jasmone

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