John Wiley & Sons, Inc. SpectraBase; SpectraBase Compound ID=IzMzuuJI3Bo

(accessed ).
Androstanolone
SpectraBase Compound ID IzMzuuJI3Bo
InChI InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12,14-17,21H,3-11H2,1-2H3/t12-,14-,15-,16-,17-,18-,19-/m0/s1
InChIKey NVKAWKQGWWIWPM-ABEVXSGRSA-N
Mol Weight 290.45 g/mol
Molecular Formula C19H30O2
Exact Mass 290.22458 g/mol
Enantiomer InChIKey NVKAWKQGWWIWPM-SSBZYEIASA-N
Copyright Copyright © 2009-2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number A2570-000
Copyright Copyright © 2015-2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample TCI Chemicals India Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number A0462
Copyright Copyright © 1980, 1981-2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich Chemical Company, Inc., Milwaukee, Wisconsin
Solvent Chloroform-d; Reference=TMS Spectrometer= Varian CFT-20
Copyright Copyright © 2016-2021 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2021 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2021 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2021 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2021 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2021 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2021 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2009-2021 John Wiley & Sons, Inc. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2015-2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample TCI Chemicals India Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number A0462
Copyright Copyright © 2013-2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number A2570-000
Copyright Copyright © 2015-2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Company LLC
Source of Spectrum Forensic Spectral Research
Catalog Number A8380
Copyright Copyright © 1980, 1981-2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich Chemical Company, Inc., Milwaukee, Wisconsin
Catalog Number A8600-7
Technique KBr WAFER
Copyright Copyright © 2015-2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample TCI Chemicals India Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number A0462
Technique KBr1
Copyright Copyright © 2008-2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids
Source of Spectrum Forensic Spectral Research
Catalog Number A2570-000
Technique KBr1 0.44mg
Copyright Copyright © 2020-2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SWG-33-2354-0
  • Stanolone
  • 5α-Androstan-17β-ol-3-one
  • 17β-Hydroxy-3-androstanone
  • (5a,17b)-17-Hydroxyandrostan-3-one
  • Dihydrotestosterone
  • Allodihydrotestosterone
  • 5α-Dihydrotestosterone
  • DHT
  • DHT;DIHYDROTESTOSTERONE
  • (5-ALPHA,17-BETA)-17-HYDROXY-3-ANDROSTANONE
  • 17b-Hydroxy-5a-androstan-3-one
  • 5A-ANDROSTAN-3-ONE, 17B-HYDROXY-,
Title Journal or Book Year
Molecular docking simulation studies on potent butyrylcholinesterase inhibitors obtained from microbial transformation of dihydrotestosterone Chemistry Central Journal 2013
A new simple and high-yield synthesis of 5α-dihydrotestosterone (DHT), a potent androgen receptor agonist Steroids 2012
An unusual ring—A opening and other reactions in steroid transformation by the thermophilic fungus Myceliophthora thermophila The Journal of Steroid Biochemistry and Molecular Biology 2009
The biotransformation of some steroids by Cephalosporium aphidicola Phytochemistry 1993
Synthesis of 17β-hydroxy-1′-H-5α-androst-2-eno[3,2-b]pyrrole and 17β-hydroxy-1′-H-5α-androst-3-eno[3,4-b]pyrrole fromO-(2-hydroxyethyl)ketoxime precursors Journal of Heterocyclic Chemistry 1990
Properties of the zinc-nickel chloride-deuterium oxide system: a simple method for deuterium addition to carbon-carbon and carbon-oxygen double bonds The Journal of Organic Chemistry 1990
13C n.m.r. spectra of steroids —a survey and commentary Organic Magnetic Resonance 1977
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