129908-91-4

Basic information

• Product Name: Acetic acid (3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-oxo-16-[1-phenyl-meth-(E)-ylidene]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester
• Synonyms: Acetic acid (3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-oxo-16-[1-phenyl-meth-(E)-ylidene]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester
• CAS NO: 129908-91-4
• Molecular Weight: 418.576
• Mol File: 129908-91-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Acetic acid (3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-oxo-16-[1-phenyl-meth-(E)-ylidene]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-oxo-16-[1-phenyl-meth-(E)-ylidene]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(129908-91-4)
• EPA Substance Registry System: Acetic acid (3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-oxo-16-[1-phenyl-meth-(E)-ylidene]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(129908-91-4)

Safety Data

• Hazardous Substances Data: 129908-91-4(Hazardous Substances Data)

Upstream product

• 853-23-6 prasterone acetate 
• 100-52-7 benzaldehyde 
• 53-43-0 dehydroepiandrosterone 
• 17243-87-7 16-benzylidene-17-oxo-5-androsten-3β-ol 
• 108-24-7 acetic anhydride 

Downstream Products

• 129909-06-4 Acetic acid (5bR,9S,11aR,11bS,13aS)-11a,13a-dimethyl-4-[1-phenyl-meth-(E)-ylidene]-4,5,5a,5b,6,8,9,10,11,11a,11b,12,13,13a-tetradecahydro-1,2,3,13b-tetraaza-cyclopenta[a]chrysen-9-yl ester 
• 129909-11-1 Acetic acid (3S,8R,9S,10R,13S,14S)-17-[(E)-hydroxyimino]-10,13-dimethyl-16-[1-phenyl-meth-(E)-ylidene]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester 
• 129908-96-9 Acetic acid (4bR,8S,10aR,10bS,12aS)-10a,12a-dimethyl-2-oxo-3-[1-phenyl-meth-(E)-ylidene]-1,2,3,4,4a,4b,5,7,8,9,10,10a,10b,11,12,12a-hexadecahydro-1-aza-chrysen-8-yl ester 

Relevant articles and documents

Synthesis of steroidal pyrimidines

Selected aryl aldehydes were treated with 17-oxo-5-androsten-3β-yl acetate (I) to give the corresponding 16-arylidene 17-oxo-5-androsten-3β-yl acetates (IIa-e). Condensation of these chalcones with urea revealed the formation of the corresponding substituted pyrimidin-2'-ones (IIIa-e) respectively.

Schmidt reaction of steroidal chalcones and Beckmann reaction of the corresponding ketoximes

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