2324-11-0

Basic information

• Product Name: (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL
• Synonyms: (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL
• CAS NO: 2324-11-0
• Molecular Formula: C₂₁H₃₄O₃
• Molecular Weight: 334.497
• Mol File: 2324-11-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 183-185 °C
• Boiling Point: 426.8±18.0 °C(Predicted)
• Appearance: /
• Density: 1.10±0.1 g/cm3(Predicted)
• PKA: 15.11±0.70(Predicted)
• CAS DataBase Reference: (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL(CAS DataBase Reference)
• NIST Chemistry Reference: (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL(2324-11-0)
• EPA Substance Registry System: (3,5,17)-17-ACETATE ANDROSTANE-3,17-DIOL(2324-11-0)

Safety Data

• Hazardous Substances Data: 2324-11-0(Hazardous Substances Data)

Upstream product

• 1852-53-5 androstanediol 
• 64-19-7 acetic acid 
• 39012-39-0 Acetic acid (3R,5S,10S,13S,17S)-10,13-dimethyl-3-(toluene-4-sulfonyloxy)-hexadecahydro-cyclopenta[a]phenanthren-17-yl ester 
• 39012-39-0 3β-Tosyloxy-17β-acetoxy-5α-androstan 
• 1164-91-6 stanolone acetate 
• 108-24-7 acetic anhydride 
• 110-86-1 pyridine 

Downstream Products

• 1164-91-6 stanolone acetate 

Relevant articles and documents

STEREOSELECTIVE REDUCTION OF C-2 SUBSTITUTED STEROID C-3 KETONES WITH LITHIUM TRIS-(R,S-1,2-DIMETHYLPROPYL)-BOROHYDRIDE AND SODIUM BOROHYDRIDE

The effect of C-2 substitution on the stereoselective reduction of steroid C-3 ketones with lithium tris(R,S-1,2-dimethylpropyl)-borohydride and sodium borohydride was investigated.The C-2 mono- and di-substituted chloro and methyl derivatives were predominantly reduced to one of the epimeric alcohols.The 2α-chloro and 2α-methyl derivatives of 17β-acetoxy-5α-androstan-3-one undergo stereoselective reduction with lithium tris (R,S-1,2-dimethylpropyl)-borohydride to the axial (3α) alcohol as observed in the unsubstituted compound, whereas sodium borohydride gives predominantly the equatorial (3β) alcohol.The 2β-chloro, 2β-methyl, 2,2-dichloro, and 2,2-dimethyl derivatives are reduced predominantly to the equatorial (3β) alcohol by both reagents.

Analysis of 5alpha-androstanediol monoacetates by thin-layer and gas-liquid chromatography and mass spectrometry.

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