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acetic acid [(1S,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-decalin-1-yl]methyl ester

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

acetic acid [(1S,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-decalin-1-yl]methyl ester
SpectraBase Compound ID HcvY0pbIWLo
InChI InChI=1S/C17H30O3/c1-12(18)20-11-14-16(4)9-6-8-15(2,3)13(16)7-10-17(14,5)19/h13-14,19H,6-11H2,1-5H3/t13-,14+,16-,17+/m0/s1
InChIKey VSZSBPFFXQATCL-HDEZJCGLSA-N
Mol Weight 282.42 g/mol
Molecular Formula C17H30O3
Exact Mass 282.219495 g/mol
Enantiomer InChIKey VSZSBPFFXQATCL-WTTBNOFXSA-N

View Spectrum of acetic acid [(1S,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-decalin-1-yl]methyl ester

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum F-49-10408-5

View Spectrum of acetic acid [(1S,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-decalin-1-yl]methyl ester

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum F-51-7443-18

View Spectrum of acetic acid [(1S,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-decalin-1-yl]methyl ester

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • [(1S,2R,4aS,8aS)-2,5,5,8a-tetramethyl-2-oxidanyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl ethanoate
1-Naphthalenemethanol, decahydro-2-hydroxy-2,5,5,8a-tetramethyl-, .alpha.-acetate, [1S-(1.alpha.,2.beta.,4a.beta.,8a.alpha.)]-
1-ACETOXYMETHYL-2,5,5,8A-TETRAMETHYL-2-HYDROXY-TRANS-DECALINE
2-[(2R,8aS)-2-hydroxy-2,5,5,8a-tetramethyldecahydro-1-naphthalenyl]ethyl phenylcarbamate
(12E)-8-HYDROXY-15-NOR-12-LABDEN-14-AL
2-BUTENAL, 4-(DIHYDRO-2-HYDROXY-2,5,5,8A-TETRAMETHYL-1-NAPHTHALENYL)-2
(1R,2R,8aS)-2,5,5,8a-tetramethyl-1-[(2Z)-3-methylpenta-2,4-dienyl]-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol
(12E)-Abienol
(CIS)-ABIENOL
Z-(1R,2R,4aS,8aS)-2,5,5,8a-tetramethyl-1-(3-methylpenta-2-en-1-yl)decahydronaphthalen-2-ol
Labd-13(E)-ene-8a,15-diol-15-yl acetate
Title Journal or Book Year
Cyclization and Rearrangements of Farnesol and Nerolidol Stereoisomers in Superacids The Journal of Organic Chemistry 1994
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