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YVCUGZBVCHODNB-WEDXCCLWSA-N
SpectraBase Compound ID 7eM6PPmQm3M
InChI InChI=1S/C10H18O2/c1-9(2)7-4-5-10(3,12-9)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8+,10+/m1/s1
InChIKey YVCUGZBVCHODNB-WEDXCCLWSA-N
Mol Weight 170.25 g/mol
Molecular Formula C10H18O2
Exact Mass 170.13068 g/mol
Enantiomer InChIKey YVCUGZBVCHODNB-QXFUBDJGSA-N
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Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Solvent CDCL3
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 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 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 CDCl3
  • 2-ALPHA-HYDROXYCINEOLE
  • 2-ALPHA-HYDROXY-1,8-CINEOLE
  • (+/-)-2-EXO-HYDROXY-CINEOLE
  • (1S,4R,6R)-1,3,3-TRIMETHYL-2-OXA-BICYCLO-[2.2.2]-OCTAN-6-OL;2-ENDO-HYDROXYCINEOLE
  • 1,3,3-TRIMETHYL-2-OXABICYCLO-[2.2.2]-OCT-6-OL
  • (-)-(1S,4R,6R)-1,3,3-Trimethyl-2-oxabicyclo-[2.2.2]-octan-6-ol
  • 1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octan-6-ol (D2)
Title Journal or Book Year
The 3-Hydroxycineoles Australian Journal of Chemistry 2005
Two New Biocatalysts for Improved Biological Oxidation of 1,8-Cineole Australian Journal of Chemistry 2005
Biotransformation of 1,8-cineole by cultured cells of Eucalyptus perriniana Phytochemistry 1994
2,9-Dihydroxy- and 2,10-Dihydroxy-1,8-cineole. Two New Possum Urinary Metabolites Australian Journal of Chemistry 1994
Halogenated terpenoids. XX. The seven monochlorocineoles Australian Journal of Chemistry 1983
Eucalyptus as biomass. Novel compounds from microbial conversion of 1,8-cineole. Agricultural and Biological Chemistry 1982

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