19324-98-2

Basic information

• Product Name: 3β,16α-dihydroxy-5α-androstan-17-one diacetate
• CAS NO: 19324-98-2
• Molecular Weight: 390.52
• Mol File: 19324-98-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3β,16α-dihydroxy-5α-androstan-17-one diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 3β,16α-dihydroxy-5α-androstan-17-one diacetate(19324-98-2)
• EPA Substance Registry System: 3β,16α-dihydroxy-5α-androstan-17-one diacetate(19324-98-2)

Safety Data

• Hazardous Substances Data: 19324-98-2(Hazardous Substances Data)

Upstream product

• 108-20-3 di-isopropyl ether 
• 23457-53-6 3β,17β-diacetoxy-16α,17α-epoxy-5α-androstane 
• 481-29-8 Epiandrosterone 
• 23357-25-7 3β,16α-diacetoxy-17-hydroxy-pregn-5-en-20-one 
• 110-86-1 pyridine 
• 67-56-1 methanol 
• 7664-93-9 sulfuric acid 
• 108-24-7 acetic anhydride 
• 1239-31-2 3β-acetoxy-5α-androstan-17-one 
• 2570-63-0 thallium(III) acetate 
• 76389-45-2 3β,16α-Diacetoxy-5α-androstan-17-on-(E)-oxim 
• 1247-67-2 3β,17-Diacetoxy-5α-androsten-(16) 
• 69389-77-1 3β,16α-diacetoxy-17-hydroxy-5α-pregnan-20-one 

Downstream Products

• 1159-67-7 3β,16α-dihydroxy-5α-androstan-17-one 
• 103327-64-6 3β,16α-bis-benzoyloxy-5α-androstane 
• 22630-49-5 3β,16α-dihydroxy-5α-androstane 

Relevant articles and documents

A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of α,β-unsaturated ketoximes

The reaction of α,β-unsaturated ketoximes with fluoroalkanosulfonyl fluorides in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) underwent the Beckmann rearrangement smoothly to afford the corresponding acid-sensitive enamides in moderate to excellent yields, which provides a new efficient method for the preparation of acid-sensitive enamides.

The in vivo metabolism of 16-alpha-hydroxydehydroisoandrosterone in man.

-