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2-BETA,4-DIHYDROXY-1,8-CINEOLE;1,3,3-TRIMETHYL-2-OXABICYCLO-[2.2.2]-OCTANE-2-BETA,4-DIOL

Compound with spectra: 2 NMR, and 1 MS (GC)

2-BETA,4-DIHYDROXY-1,8-CINEOLE;1,3,3-TRIMETHYL-2-OXABICYCLO-[2.2.2]-OCTANE-2-BETA,4-DIOL
SpectraBase Compound ID KSJ9ggzfHH2
InChI InChI=1S/C10H18O3/c1-8(2)10(12)5-4-9(3,13-8)7(11)6-10/h7,11-12H,4-6H2,1-3H3/t7-,9+,10+/m1/s1
InChIKey PEWQMISWINPIPZ-JEZHCXPESA-N
Mol Weight 186.25 g/mol
Molecular Formula C10H18O3
Exact Mass 186.125594 g/mol
Enantiomer InChIKey PEWQMISWINPIPZ-FXBDTBDDSA-N

View Spectrum of 2-BETA,4-DIHYDROXY-1,8-CINEOLE;1,3,3-TRIMETHYL-2-OXABICYCLO-[2.2.2]-OCTANE-2-BETA,4-DIOL

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum B-47-2087-0

View Spectrum of 2-BETA,4-DIHYDROXY-1,8-CINEOLE;1,3,3-TRIMETHYL-2-OXABICYCLO-[2.2.2]-OCTANE-2-BETA,4-DIOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 2-BETA,4-DIHYDROXY-1,8-CINEOLE;1,3,3-TRIMETHYL-2-OXABICYCLO-[2.2.2]-OCTANE-2-BETA,4-DIOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
  • (1S,2R,4S)-2,4-DIHYDROXY-1,8-CINEOLE
  • 2b,4-dihydroxy-1,8-cineole
2-ALPHA,4-DIHYDROXY-1,8-CINEOLE;1,3,3-TRIMETHYL-2-OXABICYCLO-[2.2.2]-OCTANE-2-ALPHA,4-DIOL
(1R,2R,4R)-2,4-DIHYDROXY-1,8-CINEOLE
(1R)-5.alpha.,6.alpha.a-Dihydroxycineole
(1S,2S,4S,5R)-2,4-DIHYDROXY-1,8-CINEOLE
(1S,2R,4S,5R)-2,4-DIHYDROXY-1,8-CINEOLE
(3R,6R)-2,2,6-trimethyl-6-(4-methylenecyclohex-2-enyl)tetrahydro-2H-pyran-3-ol
6,8-Dimethyl-2,7-dioxatricyclo[4.2.1.0(3,8)]nonane
exo-5-hydroxy-1,3-dimethyl-2-oxabicyclo[2.2.2]octan-3-methanol
YOLNCNSIZAMMOX-DEFSSGQSSA-N
(1R,3S,4R,6S)-3-Hydroxy-9-methoxy-4,9-dimethyl-7-oxabicyclo[4.3.0]nonane isomer
Title Journal or Book Year
Water-Soluble Constituents of Fennel. VI. 1,8-Cineole Type Glycosides. Chemical and Pharmaceutical Bulletin 1998
2-α,4-Dihydroxy-1,8-cineole. A New Possum Urinary Metabolite Australian Journal of Chemistry 1994
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