115350-45-3

Basic information

• Product Name: 3β-acetoxy-5α,6α-epoxy-androst-17-one, ethylene ketal
• Synonyms: 3β-acetoxy-5α,6α-epoxy-androst-17-one, ethylene ketal
• CAS NO: 115350-45-3
• Molecular Weight: 390.52
• Mol File: 115350-45-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3β-acetoxy-5α,6α-epoxy-androst-17-one, ethylene ketal(CAS DataBase Reference)
• NIST Chemistry Reference: 3β-acetoxy-5α,6α-epoxy-androst-17-one, ethylene ketal(115350-45-3)
• EPA Substance Registry System: 3β-acetoxy-5α,6α-epoxy-androst-17-one, ethylene ketal(115350-45-3)

Safety Data

• Hazardous Substances Data: 115350-45-3(Hazardous Substances Data)

Upstream product

• 14456-20-3 3β-acetoxy-5-androsten-17-one-17-ethyleneketal 

Downstream Products

• 2283-82-1 3α-hydroxy-androst-5-en-17-one 
• 14167-51-2 5-androstene-3α,16α-diol-17-one 
• 1016226-71-3 16α-bromo-5-androst-5-ene-17-one-3α-ol 
• 18386-45-3 3β-Hydroxyandrost-4-ene-6,17-dione 

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.