1259-22-9

Basic information

• Product Name: 5-androstene-3β,17β-diol 3-acetate 17-p-toluene-δ-sulfonate
• Synonyms: 5-androstene-3β,17β-diol 3-acetate 17-p-toluene-δ-sulfonate
• CAS NO: 1259-22-9
• Molecular Weight: 486.673
• Mol File: 1259-22-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-androstene-3β,17β-diol 3-acetate 17-p-toluene-δ-sulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 5-androstene-3β,17β-diol 3-acetate 17-p-toluene-δ-sulfonate(1259-22-9)
• EPA Substance Registry System: 5-androstene-3β,17β-diol 3-acetate 17-p-toluene-δ-sulfonate(1259-22-9)

Safety Data

• Hazardous Substances Data: 1259-22-9(Hazardous Substances Data)

Upstream product

• 853-23-6 prasterone acetate 
• 1639-43-6 androstenediol-3-acetate 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 481-30-1 epitestosterone 
• 36025-82-8 3-oxoandrost-4-en-17α-yl benzoate 
• 571-24-4 5alpha-Androstane-17alpha-ol-3-one 
• 40768-03-4 androst-5-ene-3β,17α-diyl 3-acetate 17-benzoate 
• 5692-03-5 5beta-Androstane-17alpha-ol-3-one 
• 150054-83-4 3β-hydroxy-5α-androstan-17α-yl cyclohexanecarboxylate 
• 103133-50-2 3-oxo-5α-androstan-17α-yl cyclohexanecarboxylate 
• 40768-04-5 3β-hydroxyandrost-5-en-17α-yl benzoate 
• 27833-18-7 17β-hydroxy-1,4-androstadien-3-one. 
• 150054-81-2 3-oxoandrosta-1,4-dien-17α-yl benzoate 
• 150054-87-8 5α-androstane-3β,17α-diyl 3-p-toluenesulfonate 17-cyclohexanecarboxylate 
• 150054-88-9 3α-hydroxy-5α-androstan-17α-yl 17-cyclohexanecarboxylate 
• 150054-84-5 Cyclohexanecarboxylic acid (3S,5R,8R,9S,10S,13S,14S,17R)-3-hydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-17-yl ester 
• 150054-85-6 3-oxo-5β-androstan-17α-yl cyclohexanecarboxylate 

Relevant articles and documents

Synthesis of novel 17-triazolyl-androst-5-en-3-ol epimers via Cu(I)-catalyzed azide-alkyne cycloaddition and their inhibitory effect on 17α-hydroxylase/C17,20-lyase

The regioselective Cu(I)-catalyzed 1,3-dipolar cycloaddition of 17α- and 17β-azidoandrost-5-en-3β-ol epimers (3b and 5b) with different terminal alkynes afforded novel 1,4-substituted triazolyl derivatives (8a–k and 9a–k). For the preparation of 5′-iodo-1

Steroids. XXVII. Neighbouring group participation. IV. Preparation of 16α-hydroxymethylandrost-5-ene-3β,17α-diol

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