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8,15-DIHYDROXY-13E-LABDANE

Compound with spectra: 3 NMR, and 2 MS (GC)

8,15-DIHYDROXY-13E-LABDANE
SpectraBase Compound ID BuetvdIbJ7g
InChI InChI=1S/C20H36O2/c1-15(10-14-21)7-8-17-19(4)12-6-11-18(2,3)16(19)9-13-20(17,5)22/h10,16-17,21-22H,6-9,11-14H2,1-5H3/b15-10+/t16-,17+,19-,20+/m0/s1
InChIKey LEOHDQKUMQKLMP-NUKBDRAPSA-N
Mol Weight 308.5 g/mol
Molecular Formula C20H36O2
Exact Mass 308.27153 g/mol
Enantiomer InChIKey LEOHDQKUMQKLMP-BVVYIIRBSA-N

View Spectrum of 8,15-DIHYDROXY-13E-LABDANE

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 Adams' Essential Oil Components (GC-MS), Version 4

View Spectrum of 8,15-DIHYDROXY-13E-LABDANE

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Adams' Essential Oil Components (GC-MS), Version 4

View Spectrum of 8,15-DIHYDROXY-13E-LABDANE

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

View Spectrum of 8,15-DIHYDROXY-13E-LABDANE

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

View Spectrum of 8,15-DIHYDROXY-13E-LABDANE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
  • LABD-(13E)-ENE-8-ALPHA,15-DIOL
  • (+/-)-(13E)-13-LABDENE-8-ALPHA,15-DIOL
  • Labd-13E-8,15-diol
Vulgarol
Labd-13E-8,15-diol
(.+-.)-(13E)-Labd-13-ene-8a,15-diol
LABD-13(Z)-ENE-8-ALPHA,15-DIOL
Z-LABD-13-ENE-8A,15-DIOL
LEOHETERONIN-D;LABD-13-ENE-8,15-DIOL
2-NAPHTHALENOL, 1-[(5-(ACETYLOXY)-3-METHYL)-3-PENTENYL]-DECAHYDRO-2,5,
2-NAPHTHALENOL, DECAHYDRO-2,5,5,8A-TETRAMETHYL-1-(3-METHYL-3-PENTENYL)
(Z)-LABD-13-EN-8-ALPHA-OL
8-Hydroxy-trans-13-labden-15-carboxylic acid, methyl ester
14,15-Dinor-8.alpha.-hydroxy-13-labdanone
Title Journal or Book Year
A diterpene from Cipadessa fruticosa and Grangea maderaspatana Phytochemistry 1994
Chemical simulation of polycyclic diterpenoid biosynthesis using mercury(II) triflate/N,N-dimethylaniline complex: mechanistic aspects of a biomimetic olefin cyclization The Journal of Organic Chemistry 1986

This compound is available in the following databases:

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Labd-13E-8,15-diol
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