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(+)-Dihydrocholesterol

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

(+)-Dihydrocholesterol
SpectraBase Compound ID 5bCN1sRJq3L
InChI InChI=1S/C27H48O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-25,28H,6-17H2,1-5H3/t19-,20?,21?,22+,23-,24+,25+,26+,27-/m1/s1
InChIKey QYIXCDOBOSTCEI-BPAAZKTESA-N
Mol Weight 388.7 g/mol
Molecular Formula C27H48O
Exact Mass 388.370516 g/mol
Enantiomer InChIKey QYIXCDOBOSTCEI-HXDBWITKSA-N

View Spectrum of (+)-Dihydrocholesterol

MS (GC) Spectrum
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Prof. D. Henneberg, MPI f. Kohlenforschung, Muelheim a.d.R., Germany

View Spectrum of (+)-Dihydrocholesterol

ATR-IR Spectrum
Copyright Copyright © 2018-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich
Catalog Number D104604

View Spectrum of (+)-Dihydrocholesterol

13C NMR Spectrum
Copyright Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number D104604
Solvent CDCl3

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1H NMR Spectrum
Copyright Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number D104604
Solvent CDCl3

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FTIR Spectrum
Copyright Copyright © 2018-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number D104604
Technique Mull

View Spectrum of (+)-Dihydrocholesterol

Raman Spectrum
Copyright Copyright © 2017-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2017-2024 John Wiley & Sons, Inc. All Rights Reserved.
Catalog Number D104604
  • CHOLESTAN-3-OL
  • (1S,2S,10R,11S,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0(2,7).0(11,15)]heptadecan-5-ol
  • DIHYDROCHOLESTENOL
Coprosterol
5b-Cholestan-3b-ol
5.alpha.-Cholestan-3.alpha./.beta.-ol
5a-Cholestan-3b-ol
5a-Cholestan-3a-ol
5b-Cholestan-3a-ol
CHOLESTAN-3-OL, (3.BETA.)-
CHOLESTAN-3-BETA-OL
CHOLESTAN-3-ALPHA-OL
(20S)-20-Iso-5.alpha.-cholestan-3.beta.-ol
Epicoprostanol
Epicoprostanol
3b,5b-Cholestan-3-ol
Cholestane-3,5-diol, 5-acetate, (3beta,5alpha)-
5.alpha.-Cholestan-3.beta.,26-diol
27-nor-5.alpha.-Cholestan-3.beta.-ol
(3R,5R)-10,13-Dimethyl-17-(1-methyl-4-methylsulfanyl-butyl)-hexadecahydro-cyclopenta[a]phenanthren-3-ol
(3S,5S,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-5-methylhexan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
Cholan-3-ol
(3R,5R,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(1R)-1-methyl-4-morpholino-butyl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
CHOLESTAN-3-OL, (3.BETA.)-
5a-Cholestan-3a-ol
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