calamenene (1-S,cis)

• Formula: C₁₅H₂₂
• Molecular weight: 202.3352
• IUPAC Standard InChI: InChI=1S/C15H22/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h5,7,9-10,12-13H,6,8H2,1-4H3/t12-,13-/m0/s1 Copy

  
• IUPAC Standard InChIKey: PGTJIOWQJWHTJJ-STQMWFEESA-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-Calamenene
  • cis-Calamenene
  • α-Calamenene
• Stereoisomers:
  • Naphthalene, 1,2,3,4-tetrahydro-1,6-dimethyl-4-(1-methylethyl)-, (1S-cis)-
  • trans-Calamenene
  • Calamenene I
  • Calamenene II
  • 1R-trans-calamenene
  • (1S )-(E)-Calamenene
  • 1,2,3,4-Tetrahydro-1,6-dimethyl-4-(1-methylethyl) naphthalene
  • trans-Calamenene
  • (E)-Calamenene
• Other names: 1S-cis-1,2,3,4-Tetrahydro-1,6-dimethyl-4-isopropylnaphthalene
• 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

Normal alkane RI, non-polar column, temperature ramp

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Normal alkane RI, non-polar column, custom temperature program

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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.

Cornu, Carnat, et al., 2001
Cornu, A.; Carnat, A.-P.; Martin, B.; Coulon, J.-B.; Lamaison, J.-L.; Berdagué, J.-L., Solid-phase microextraction of volatile components from natural grassland plants, J. Agric. Food Chem., 2001, 49, 1, 203-209, https://doi.org/10.1021/jf0008341 . [all data]

Ning, Zheng, et al., 2008
Ning, H.; Zheng, F.; Sun, B.; Xie, J.; Liu, Y., Solvent-free microwave extraction of essential oil from Zanthoxylum bungeanum Maxim., Food Environ. Ind. (Chinese), 2008, 34, 5, 179-184. [all data]

Notes

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