(-)-Jasmonic acid, methyl ester (trans)

• Formula: C₁₃H₂₀O₃
• Molecular weight: 224.2961
• IUPAC Standard InChI: InChI=1S/C13H20O3/c1-3-4-5-6-11-10(7-8-12(11)14)9-13(15)16-2/h4-5,10-11H,3,6-9H2,1-2H3/b5-4-/t10-,11-/m0/s1 Copy

  
• IUPAC Standard InChIKey: GEWDNTWNSAZUDX-XXJOZFEBSA-N Copy
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
  The 3d structure may be viewed using Java or Javascript.
• Species with the same structure:
  • cis-Methyl jasmonate
• Stereoisomers:
  • Methyl jasmonate
  • methyl epijasmonate
  • Cyclopentaneacetic acid, 3-oxo-2-(2-pentenyl)-, methyl ester, [1α,2α(Z)]-
  • (+)-Jasmonic acid, methyl ester (cis)
  • (+)-(Z)-Methyl epijasmonate
  • Methyl (Z)-epi-jasmonate
  • (E)-methyl jasmonate
  • Methyl epi-jasmonate
  • (Z)-Methyl epi-jasmonate
• Information on this page:
  • Gas Chromatography
  • References
  • Notes
• Options:
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Gas Chromatography

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Van Den Dool and Kratz RI, non-polar column, custom temperature program

View large format table.

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Schmidt, Kramell, et al., 1990
Schmidt, J.; Kramell, R.; Brückner, C.; Schneider, G.; Sembdner, G.; Schreiber, K.; Stach, J.; Jensen, E., Gas chromatography/mass spectrometric and tandem mass spectrometric investigations of synthetic amino acid conjugates of jasmonic acid and endogenously occurring related compunds from Vicia faba L., Biomed. Environ. Mass Spectrom., 1990, 19, 5, 327-338, https://doi.org/10.1002/bms.1200190508 . [all data]

Notes

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• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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