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3-BETA-HYDROXY-1,8-CINEOLE
SpectraBase Compound ID LZtjVnAUS65
InChI InChI=1S/C10H18O2/c1-9(2)7-4-5-10(3,12-9)6-8(7)11/h7-8,11H,4-6H2,1-3H3/t7-,8+,10+/m1/s1
InChIKey WHIKIYRWRMRQNK-WEDXCCLWSA-N
Mol Weight 170.25 g/mol
Molecular Formula C10H18O2
Exact Mass 170.13068 g/mol
Enantiomer InChIKey WHIKIYRWRMRQNK-QXFUBDJGSA-N
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCL3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (+/-)-3-ENDO-HYDROXY-CINEOLE
  • (1R/S,4S/R,5R/S)-1,3,3-TRIMETHYL-2-OXABICYCLO-[2.2.2]-OCTAN-5-OL;RACEMIC-(1R/S,3R/S,4S/R)-3-HYDROXYCINEOLE
  • (1RS,4SR,5RS)-1,3,3-TRIMETHYL-2-OXABICYCLO-[2.2.2]-OCTAN-5-OL
Title Journal or Book Year
The 3-Hydroxycineoles Australian Journal of Chemistry 2005
2,9-Dihydroxy- and 2,10-Dihydroxy-1,8-cineole. Two New Possum Urinary Metabolites Australian Journal of Chemistry 1994
Halogenated Terpenoids. XXIV. The Bromocineoles Australian Journal of Chemistry 1986
Eucalyptus as biomass. Novel compounds from microbial conversion of 1,8-cineole. Agricultural and Biological Chemistry 1982

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