111992-94-0

Basic information

• Product Name: benzyl 3α,7α-dihydroxy-5β-cholan-24-oate
• Synonyms: benzyl 3α,7α-dihydroxy-5β-cholan-24-oate
• CAS NO: 111992-94-0
• Molecular Weight: 482.704
• Mol File: 111992-94-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: benzyl 3α,7α-dihydroxy-5β-cholan-24-oate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 3α,7α-dihydroxy-5β-cholan-24-oate(111992-94-0)
• EPA Substance Registry System: benzyl 3α,7α-dihydroxy-5β-cholan-24-oate(111992-94-0)

Safety Data

• Hazardous Substances Data: 111992-94-0(Hazardous Substances Data)

Upstream product

• 474-25-9 chenodeoxycholic acid 
• 100-39-0 benzyl bromide 

Downstream Products

• 907205-58-7 Pyrene-1-carboxylic acid (3R,5R,7R,8R,9S,10S,13R,14S,17R)-17-((R)-3-benzyloxycarbonyl-1-methyl-propyl)-7-hydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester 
• 907205-61-2 Pyrene-1-carboxylic acid (3R,5S,7R,8R,9S,10S,13R,14S,17R)-17-((R)-3-benzyloxycarbonyl-1-methyl-propyl)-10,13-dimethyl-7-(2-1,4,7,10,13-pentaoxa-16-aza-cyclooctadec-16-yl-acetoxy)-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester 
• 907205-62-3 Pyrene-1-carboxylic acid (3R,5S,7R,8R,9S,10S,13R,14S,17R)-17-((R)-3-benzyloxycarbonyl-1-methyl-propyl)-10,13-dimethyl-7-(2-1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl-acetoxy)-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester 
• 907205-60-1 Pyrene-1-carboxylic acid (3R,5S,7R,8R,9S,10S,13R,14S,17R)-17-((R)-3-benzyloxycarbonyl-1-methyl-propyl)-7-(2-chloro-acetoxy)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester 

Relevant articles and documents

A simple and general strategy for the design of fluorescent cation sensor beads

Chenodeoxycholic acid based PET sensors for alkali metal ions have been immobilized on Merrifield resin and on Tentagel. The fluorescence of the sensor beads is enhanced upon binding the cations. The modular nature of the sensor allows designing different

Obeticholic acid structural analogue as well as preparation method and application thereof

The invention discloses an obeticholic acid structural analogue. The obeticholic acid structural analogue is 3alpha,7alpha-dihydroxy-23-ethyl-5beta-ursodeoxycholic acid (II). The invention further discloses a preparation method of the obeticholic acid str