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5-ALPHA-CHOLESTAN-5-OL
SpectraBase Compound ID 7lzBDfHbrdP
InChI InChI=1S/C27H48O/c1-19(2)9-8-10-20(3)22-11-12-23-21-13-18-27(28)16-7-6-15-26(27,5)24(21)14-17-25(22,23)4/h19-24,28H,6-18H2,1-5H3/t20-,21+,22-,23+,24+,25-,26-,27+/m1/s1
InChIKey LJSXUKQWGACPQQ-QKWCZOFSSA-N
Mol Weight 388.7 g/mol
Molecular Formula C27H48O
Exact Mass 388.370516 g/mol
Enantiomer InChIKey LJSXUKQWGACPQQ-XCMUPAKZSA-N
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Prof. Spiteller, University Bayreuth, Germany
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 CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 5a-Cholestanol
  • 5.ALPHA.-HYDROXY-CHOLESTAN
  • (5S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-5-ol
  • CHOLESTAN-5-OL
Title Journal or Book Year
Carbon-13 N.M.R. studies of 5α- and 5β-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols Australian Journal of Chemistry 1981
Dehydration Studies of r-4-Chloro-8a-methyl-trans- and cis-decahydronaphthalen-t-4a-ols Australian Journal of Chemistry 1979
13C n.m.r. spectra of steroids —a survey and commentary Organic Magnetic Resonance 1977
Carbon-13 nuclear magnetic resonance spectra of hydroxy steroids The Journal of Organic Chemistry 1976

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