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(+)-CAROTOL

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

(+)-CAROTOL
SpectraBase Compound ID KgZ7oRscDjg
InChI InChI=1S/C15H26O/c1-11(2)13-7-9-14(4)8-5-12(3)6-10-15(13,14)16/h5,11,13,16H,6-10H2,1-4H3/t13-,14+,15+/m1/s1
InChIKey XZYQCFABZDVOPN-ILXRZTDVSA-N
Mol Weight 222.37 g/mol
Molecular Formula C15H26O
Exact Mass 222.198365 g/mol
Enantiomer InChIKey XZYQCFABZDVOPN-RRFJBIMHSA-N

View Spectrum of (+)-CAROTOL

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 (+)-CAROTOL

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 Sample SAFC Cat.no. W224405
Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)

View Spectrum of (+)-CAROTOL

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 (+)-CAROTOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • Carotol
  • 3a(1H)-Azulenol, 2,3,4,5,8,8a-hexahydro-6,8a-dimethyl-3-(1-methylethyl)-, (3R,3aS,8aR)-
3a(1H)-Azulenol, 2,3,4,5,8,8a-hexahydro-6,8a-dimethyl-3-(1-methylethyl)-, [3R-(3.alpha.,3a.alpha.,8a.alpha.)]-
(+)-Acoren-7.alpha.-ol
1,4-Dimethyl-4-[4-(hydroxymethyl)-3,4-epoxypentyl]-5,5-(ethylenedioxy)cycloheptene
ACANTHOLIDE-D
EPIMUQUBILIN-B
Dolabella-3,8(17)-diene-7,18-diol
Eremophil-7(11)-en-10-.beta.-ol
(trans,anti,cis)-1-Methyl-2-hydroxytricyclo[7.2.0.0(2,7)]undecane
(1R,2R,4S)-2-endo-Hydroxy-2-exo-((Z)-2-butenyl)-1,3,3-trimethylbicyclo[2.2.1]heptane
(1-R,3-E,7-E,11-S,12-R)-DOLABELLA-3,7,18-TRIEN-9-ONE
Title Journal or Book Year
The role of germacrene D as a precursor in sesquiterpene biosynthesis: investigations of acid catalyzed, photochemically and thermally induced rearrangements Phytochemistry 2000
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