121058-06-8

Basic information

• Product Name: 3β,4β,17β-triacetoxy-9,10-seco-androst-5(10)-en-9-one
• CAS NO: 121058-06-8
• Molecular Weight: 448.557
• Mol File: 121058-06-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3β,4β,17β-triacetoxy-9,10-seco-androst-5(10)-en-9-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3β,4β,17β-triacetoxy-9,10-seco-androst-5(10)-en-9-one(121058-06-8)
• EPA Substance Registry System: 3β,4β,17β-triacetoxy-9,10-seco-androst-5(10)-en-9-one(121058-06-8)

Safety Data

• Hazardous Substances Data: 121058-06-8(Hazardous Substances Data)

Upstream product

• 97831-61-3 androst-4-ene-3β,9α,17β-triol 3,17-diacetate 
• 94441-33-5 androst-4-ene-3β,9α,17β-triol 
• 560-62-3 9-alpha-hydroxyandrost-4-ene-3,17-dione 

Relevant articles and documents

FREE-RADICAL OXIDATIVE TRANSFORMATIONS OF ANDROST-4-ENE-3β,9α,17β-TRIOL 3,17-DIACETATE

The oxidation of androst-4-ene-3β,9α,17β-triol 3,17-diacetate (2) with lead tetraacetate resulted mainly in β-fragmentation of the C(9)-C(10) bond to give a mixture of 10α- and 10β-acetoxy-Δ4-unsaturated 9,10-seco-steroidal ketones (3a and 3b) as the minor components (in ca.7percent yield) and the rearranged 4β-acetoxy-Δ5(10)-unsaturated 9,10-seco-9-ketone (4) as the major product (in 61percent yield).Unexpestedly, when the same substrate (2) was subjected to the mercuric oxide - iodine oxidation, it underwent predominantly α-epoxidation of the olefinic double bond to produce the 4α,5α-epoxy derivative (5) (in 58percent yield).