929270-02-0

Basic information

• Product Name: (3S,6aR,6bS,9aS,11aS,11bR)-9a,11b-dimethyl-9-oxohexadecahydrocyclopenta[1,2]phenanthro[8a,9-b]oxiren-3-yl acetate
• Synonyms: (3S,6aR,6bS,9aS,11aS,11bR)-9a,11b-dimethyl-9-oxohexadecahydrocyclopenta[1,2]phenanthro[8a,9-b]oxiren-3-yl acetate
• CAS NO: 929270-02-0
• Molecular Weight: 346.467
• Mol File: 929270-02-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3S,6aR,6bS,9aS,11aS,11bR)-9a,11b-dimethyl-9-oxohexadecahydrocyclopenta[1,2]phenanthro[8a,9-b]oxiren-3-yl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,6aR,6bS,9aS,11aS,11bR)-9a,11b-dimethyl-9-oxohexadecahydrocyclopenta[1,2]phenanthro[8a,9-b]oxiren-3-yl acetate(929270-02-0)
• EPA Substance Registry System: (3S,6aR,6bS,9aS,11aS,11bR)-9a,11b-dimethyl-9-oxohexadecahydrocyclopenta[1,2]phenanthro[8a,9-b]oxiren-3-yl acetate(929270-02-0)

Safety Data

• Hazardous Substances Data: 929270-02-0(Hazardous Substances Data)

Upstream product

• 853-23-6 prasterone acetate 

Relevant articles and documents

SYNTHESIS OF UNSATURATED CARBONYL COMPOUNDS VIA A CHROMIUM-MEDIATED ALLYLIC OXIDATION BY 70percent TERT.BUTYLHYDROPEROXIDE

Alkenes were converted into α,β-unsaturated carbonyl compounds using excess of tert.butylhydroperoxide and catalytic amounts of chromiumVI oxide at room temperature.Fair yields and conversions were obtained from Δ5-steroids while allylic oxidation of acyclic alkenes was less efficient.Epoxidation of the double bond, sometimes observed, remained a minor reaction pathway.