Linalool oxide

• Formula: C₁₀H₁₈O₂
• Molecular weight: 170.2487
• IUPAC Standard InChI: InChI=1S/C10H18O2/c1-5-10(4)7-6-8(12-10)9(2,3)11/h5,8,11H,1,6-7H2,2-4H3 Copy

  
• IUPAC Standard InChIKey: BRHDDEIRQPDPMG-UHFFFAOYSA-N Copy
• CAS Registry Number: 60047-17-8
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Species with the same structure:
  • 2-Furanmethanol, 5-ethenyltetrahydro-α,α,5-trimethyl-, cis-
  • Linalool oxide #1
  • Linalool oxide #2
  • Linalool oxide (isomer I)
  • Linalool oxide (isomer II)
  • Linallol oxide isomer # 1
  • Linalool oxide isomer # 2
• Stereoisomers:
  • Linalool oxide
  • trans-Linalool oxide (furanoid)
  • Linalol oxide furanoid B
  • linalyloxide trans (II)
  • Linalool Z-furanic oxide
  • trans-Linalol oxide (furan isomer)
  • Linalool oxide 2
  • Linalool oxide-I (furanoid)
  • trans-Linalool oxide (furanoid)
  • cis-furan Linalool oxide
  • trans-furan Linalool oxide
  • cis-Linalool oxide (furan)
  • trans-α,α,5-Trimethyl-5-ethenyltetrahydro-2-furanmethanol
  • (E)-Furan linalool oxide
  • (Z)-Furan linalool oxide
  • cis-Linalool oxide I
  • trans-Linalool oxide I
  • (Z)-Linalool oxide (furanoid)
  • cis-Linalool oxde, furanoid
  • trans-Linanool oxide
• Other names: Epoxylinalool; Linalol oxide (furanoid); furan linalool oxide; 5-ethenyltetrahydro-α,α-5-trimethyl-2-furanmethanol; 2-Furanmethanol, 5-ethenyltetrahydro-α,α,5-trimethyl-; 2-(tetrahydro-5-methyl-5-vinyl-2-furyl)propan-2-ol
• Information on this page:
  • Normal alkane RI, non-polar column, custom temperature program
  • References
  • Notes
• Other data available:
  • Gas Chromatography
• Options:
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Normal alkane RI, non-polar column, custom temperature program

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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

References

Go To: Top, Normal alkane RI, non-polar column, custom temperature program, Notes

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

Profitt, Schatz, et al., 2008
Profitt, M.; Schatz, B.; Bessiere, J.-M.; Chen, C.; Soler, C.; Hossaert-McKey, M., Signalling receptivity: comparison of the emission of volatile compounds by figs of Ficus hispida before, during and after the phase of receptivity to pollinators, Symbiosis, 2008, 45, 1-10. [all data]

Proffit, 2007
Proffit, M., Mediation chimique et structuration des communautes d'hymenopteres parasites du mutualisme figuier / pollinisateur (These pour obtenir le grade de Docteur de l'Universite Montpellier II) (Dissertation), 2007. [all data]

Counet, Ouwerx, et al., 2004
Counet, C.; Ouwerx, C.; Rosoux, D.; Collin, S., Relationship between procyanidin and flavor contents of cocoa liquors from different origins, J. Agric. Food Chem., 2004, 52, 20, 6243-6249, https://doi.org/10.1021/jf040105b . [all data]

Binder and Flath, 1989
Binder, R.G.; Flath, R.A., Volatile components of pineapple guava, J. Agric. Food Chem., 1989, 37, 3, 734-736, https://doi.org/10.1021/jf00087a034 . [all data]

Swigar and Silverstein, 1981
Swigar, A.A.; Silverstein, R.M., Monoterpenes, Aldrich Chemical Company, Milwaukee, WI, USA, 1981, 130. [all data]

Notes

Go To: Top, Normal alkane RI, non-polar column, custom temperature program, References

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