88729-23-1

Basic information

• Product Name: 17β-Hydroxy-17α-methyl-5β-androstanon-(3)
• CAS NO: 88729-23-1
• Molecular Weight: 304.473
• Mol File: 88729-23-1.mol

Chemical Properties

• CAS DataBase Reference: 17β-Hydroxy-17α-methyl-5β-androstanon-(3)(CAS DataBase Reference)
• NIST Chemistry Reference: 17β-Hydroxy-17α-methyl-5β-androstanon-(3)(88729-23-1)
• EPA Substance Registry System: 17β-Hydroxy-17α-methyl-5β-androstanon-(3)(88729-23-1)

Safety Data

• Hazardous Substances Data: 88729-23-1(Hazardous Substances Data)

Upstream product

• 51057-10-4 3β-Hydroxy-17α,20-oxido-21-nor-5α-pregnane 
• 1156-83-8 3β-Hydroxy-17-methylene-5α-androstane 
• 88729-25-3 17β-Methyl-5α-androstane-3β,17α-diol 
• 143579-44-6 mestanolone 17β-sulfate pyridinium salt 

Downstream Products

• 53-39-4 oxandrolone 

Relevant articles and documents

Studies on anabolic steroids. 9. Tertiary sulfates of anabolic 17α-methyl steroids: synthesis and rearrangement

A simple and convenient method has been developed to prepare sulfates of anabolic 17β-hydroxy-17α-methyl steroids.The sulfates of methandienone, 17α-methyltestosterone, mestanolone, oxandrolone, and stanozolol were prepared.Different A-ring functions were not affected under the sulfation condition.The buffered hydrolyses of these sulfates provided the 17-epimers of the original steroids and 17,17-dimethyl-18-nor-13(14)-ene steroids, presumably via the 17-carbocations. Keywords: steroids, tertiary sulfates; 17α-methyl steroids; 17β-methyl steroids; 17,17-dimethyl-18-norandrost-13(14)-enes; NMR

Proton magnetic resonance spectra of 17ξ-hydroxy-17ξ-methyl-5ξ-androstane C-3 ketone and C-3ξ alcohol isomers in chloroform-d and pyridine-d5

17α-Hydroxy-17β-methyl-5β-androstan-3-one,17β-methyl-5α-androstane-3α ,17α-diol,17β-methyl-5α-androstane-3β,17α-diol, 17α-methyl-5β-androstane-3β,17β-diol,17β-methyl-5β-androstane- 3α,17α-diol and 17β-methyl-5β-androstane-3β,17α-diol were synthesized for the first time. 1H NMR spectra of all four 17ξ-hydroxy/17ξ-methyl C-3 ketones and all eight C-3 alcohols were recorded in chloroform-d and pyridine-d5. Pyridine-induced chemical shifts are discussed. Thin-layer chromatographic data are given.