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8.alpha.,13-epoxylabdan-15-ol

Compound with spectra: 1 NMR, and 3 MS (GC)

8.alpha.,13-epoxylabdan-15-ol
SpectraBase Compound ID HZ1Ta8r7QEn
InChI InChI=1S/C20H36O2/c1-17(2)9-6-10-19(4)15(17)8-12-20(5)16(19)7-11-18(3,22-20)13-14-21/h15-16,21H,6-14H2,1-5H3/t15-,16+,18+,19-,20+/m0/s1
InChIKey JVLOQPOJKYSOJJ-GRLGQGAKSA-N
Mol Weight 308.5 g/mol
Molecular Formula C20H36O2
Exact Mass 308.27153 g/mol
Enantiomer InChIKey JVLOQPOJKYSOJJ-QVHQYWGISA-N

View Spectrum of 8.alpha.,13-epoxylabdan-15-ol

MS (GC) Spectrum
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Spectrum FF-7-142-2 (DOI: 10.1002/ffj.2730070308)

View Spectrum of 8.alpha.,13-epoxylabdan-15-ol

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum FF-7-142-2

View Spectrum of 8.alpha.,13-epoxylabdan-15-ol

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum B-44-469-0

View Spectrum of 8.alpha.,13-epoxylabdan-15-ol

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
  • Gomerol
  • 2-((3R,4aR,6aS,10aS,10bR)-3,4a,7,7,10a-pentamethyldodecahydro-1H-benzo[f]chromen-3-yl)ethan-1-ol
13-EPI-GOMEROL
1H-Naphtho[2,1-b]pyran-3-ethanol, dodecahydro-3,4a,7,7,10a-pentamethyl-
Gomerol
1H-Naphtho[2,1-b]pyran, 3-hexyldodecahydro-3,4a,7,7,10a-pentamethyl-
8-ALPHA,13-EPOXYLABDAN-15-YL-ACETATE
2,4b,8,8,10a-Pentamethyl-2-ethyl-(perhydro)naphtho[1,2-b]pyran
2,4b,8,8,10a-Pentamethyl-2-[hydroxymethyl]-(perhydro)naphtho[1,2-b]pyran
1H-NAPHTO[2,1-b]PYRAN-3-ACETALDEHYDE, DODECAHYDRO-3,4a,7,7,10a-PENTAMETHYL-
(3aRS,5aSR,9aSR,9bSR)-Perhydro-2,2,3a,6,6,9a-phexamethylnaphtho[2,1-b]furan
Sclareol diacetate
METHYL-8-ALPHA,15-EPOXY-LABDAN-16-BETA-OATE
Title Journal or Book Year
Conversion of Manoyl Oxide Into 12-β-Hydroxymanoyl Oxide Australian Journal of Chemistry 1991

Wiley Registry of Mass Spectral Data 12th Edition
Author: Wiley

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Gomerol
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