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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
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
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum Adams' Essential Oil Components (GC-MS), Version 4
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 C5D5N
  • LABD-(13E)-ENE-8-ALPHA,15-DIOL
  • (+/-)-(13E)-13-LABDENE-8-ALPHA,15-DIOL
  • Labd-13E-8,15-diol
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

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