169898-34-4

Basic information

• Product Name: methyl 12α-hydroxy-3α-<(4-nitrophenyl)acetoxy>-5β-cholan-24-oate
• CAS NO: 169898-34-4
• Molecular Weight: 569.739
• Mol File: 169898-34-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 12α-hydroxy-3α-<(4-nitrophenyl)acetoxy>-5β-cholan-24-oate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 12α-hydroxy-3α-<(4-nitrophenyl)acetoxy>-5β-cholan-24-oate(169898-34-4)
• EPA Substance Registry System: methyl 12α-hydroxy-3α-<(4-nitrophenyl)acetoxy>-5β-cholan-24-oate(169898-34-4)

Safety Data

• Hazardous Substances Data: 169898-34-4(Hazardous Substances Data)

Upstream product

• 3245-38-3 methyl deoxycholate 
• 50434-36-1 4-nitrophenylacetyl chloride 

Downstream Products

• 169898-42-4 (R)-4-{(3R,5R,8R,9S,10S,12S,13R,14S,17R)-3-[2-(4-Amino-phenyl)-acetoxy]-12-[4-(4-amino-phenyl)-butyryloxy]-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-17-yl}-pentanoic acid methyl ester 
• 169898-41-3 (R)-4-{(3R,5R,8R,9S,10S,12S,13R,14S,17R)-3-[2-(4-Amino-phenyl)-acetoxy]-12-[3-(4-amino-phenyl)-propionyloxy]-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-17-yl}-pentanoic acid methyl ester 
• 169898-37-7 methyl 3α-<(4-nitrophenyl)acetoxy>-12α-<3-(4-nitrophenyl)propanoyloxy>-5β-cholan-24-oate 
• 169898-38-8 methyl 3α-<(4-nitrophenyl)acetoxy>-12α-<4-(4-nitrophenyl)butanoyloxy>-5β-cholan-24-oate 

Relevant articles and documents

Asymmetric synthesis of steroidal Troeger's base analogues. X-ray molecular structure of methyl 3α,12α-diazocine-2,8-bisacetoxy>-5β-cholan-24-oate

Cyclization of compound 5c in trifluoroacetic acid/hexamethylenetetramine produces Troeger's base analogue 6c in 75percent yield with 70percent diastereoselectivity.