161882-44-6

Basic information

• Product Name: Biphenyl-4-carboxylic acid (3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,12-diacetoxy-17-((R)-3-methoxycarbonyl-1-methyl-propyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-7-yl ester
• Synonyms: Biphenyl-4-carboxylic acid (3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,12-diacetoxy-17-((R)-3-methoxycarbonyl-1-methyl-propyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-7-yl ester
• CAS NO: 161882-44-6
• Molecular Weight: 686.886
• Mol File: 161882-44-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Biphenyl-4-carboxylic acid (3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,12-diacetoxy-17-((R)-3-methoxycarbonyl-1-methyl-propyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-7-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Biphenyl-4-carboxylic acid (3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,12-diacetoxy-17-((R)-3-methoxycarbonyl-1-methyl-propyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-7-yl ester(161882-44-6)
• EPA Substance Registry System: Biphenyl-4-carboxylic acid (3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,12-diacetoxy-17-((R)-3-methoxycarbonyl-1-methyl-propyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-7-yl ester(161882-44-6)

Safety Data

• Hazardous Substances Data: 161882-44-6(Hazardous Substances Data)

Upstream product

• 58822-33-6 methyl 3α,12α-diacetyloxy-7α-hydroxy-5β-cholan-24-oate 
• 14002-51-8 4-biphenyl-carboxylic acid chloride 
• 15073-97-9 methyl 3α,12α-dihydroxy-7-oxo-5β-cholate 
• 21066-20-6 methyl 7-dehydrocholate diacetate (methyl 3α,12α-diacetoxy-7-oxo-5β-cholan-24-oate) 
• 81-25-4 cholic acid 
• 1448-36-8 methyl cholate 

Downstream Products

• 161882-45-7 Biphenyl-4-carboxylic acid (3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-12-acetoxy-3-hydroxy-17-((R)-3-methoxycarbonyl-1-methyl-propyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-7-yl ester 
• 152953-43-0 Biphenyl-4-carboxylic acid (3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-12-acetoxy-3-acryloyloxy-17-((R)-3-methoxycarbonyl-1-methyl-propyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-7-yl ester 

Relevant articles and documents

Asymmetric Diels-Alder reactions of chiral acrylates of cholic acid derivatives

New steroid-based chiral auxiliaries 6, 9, and 12 have been synthesized from readily available cholic acid. These new chiral auxiliaries place the reactive and the shielding sites in a 1,5 relationship to each other. Diels-Alder reaction of cyclopentadien