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3-BETA,17-BETA-DIACETOXY-B-NORANDROST-5-ENE
SpectraBase Compound ID 3Xg207E60ya
InChI InChI=1S/C22H32O4/c1-13(23)25-16-7-9-21(3)15(11-16)12-17-18-5-6-20(26-14(2)24)22(18,4)10-8-19(17)21/h12,16-20H,5-11H2,1-4H3
InChIKey NBZFRZQCWWNNEO-UHFFFAOYSA-N
Mol Weight 360.5 g/mol
Molecular Formula C22H32O4
Exact Mass 360.23006 g/mol
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
Copyright Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved.
Source of Spectrum Copyright (C) Dr. Makin, London Hospital Medical College, UK
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 9,13-Dimethyltetracyclo[11.3.0.0(2,10).0(4,9)]hexadec-3-ene, 6,14-diacetoxy-
  • 7-NORANDROST-5-ENE-3.BETA.,17.ALPHA.-DIOL(3.BETA.,17.ALPHA.-DI-ACETATE)
Title Journal or Book Year
Microbial hydroxylation of steroids. 7. Hydroxylation of B-nortestosterone and related compounds by Rhizopus arrhizus ATCC 11145, and 13C nuclear magnetic resonance spectra of some B-norsteroids Canadian Journal of Chemistry 1981

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