1232680-84-0

Basic information

• Product Name: 3β-O-(1’,2’:3’,4’-di-O-isopropylidene-α-D-galactopyranos-6’-yl)cholest-5-ene
• Synonyms: 3β-O-(1’,2’:3’,4’-di-O-isopropylidene-α-D-galactopyranos-6’-yl)cholest-5-ene
• CAS NO: 1232680-84-0
• Molecular Weight: 628.934
• Mol File: 1232680-84-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3β-O-(1’,2’:3’,4’-di-O-isopropylidene-α-D-galactopyranos-6’-yl)cholest-5-ene(CAS DataBase Reference)
• NIST Chemistry Reference: 3β-O-(1’,2’:3’,4’-di-O-isopropylidene-α-D-galactopyranos-6’-yl)cholest-5-ene(1232680-84-0)
• EPA Substance Registry System: 3β-O-(1’,2’:3’,4’-di-O-isopropylidene-α-D-galactopyranos-6’-yl)cholest-5-ene(1232680-84-0)

Safety Data

• Hazardous Substances Data: 1232680-84-0(Hazardous Substances Data)

Upstream product

• 1182-65-6 cholesteryl p-toluenesulfonate 
• 4064-06-6 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 2867-93-8 6β-methoxy-3α,5-cyclo-5-α-cholestane 
• 465-54-3 3,5-cyclocholesterol 
• 24352-63-4 17-(1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1Hcyclopenta[a]phenanthren-3-yl diphenyl phosphate 
• 1456599-09-9 6β-p-tolylsulfanyl-3α,5α-cyclocholestane 
• 79327-32-5 6β-phenylsulfanyl-3α,5α-cyclocholestane 
• 76-05-1 trifluoroacetic acid 

Relevant articles and documents

3α,5α-Cyclocholestan-6β-yl ethers as donors of the holesterol moiety for the electrochemical synthesis f cholesterol glycoconjugates

3α,5α-Cyclocholestan-6β-yl alkyl and aryl ethers were proved to be efficient cholesteryl donors in the electrochemical synthesis of glycoconjugates. 3α,5α-Cyclocholestan-6β-ol (i-cholesterol) and its tert-butyldimethylsilyl ether can also be used for this

Electrochemical synthesis of glycoconjugates of 3β-hydroxy- Δ5-steroids by using non-activated sugars and steroidal thioethers

A new protocol for the electrochemical synthesis of glycoconjugates is presented. Thioether derivatives of cholesterol and other sterols were subjected to anodic oxidation in the presence of a sugar alcohol affording glycoconjugates with the sugar linked to a steroid moiety by an ether bond. The isomeric 6β-3α,5α-cyclo-steroidal thioethers proved to be better sterol donors than the normal 3β-Δ5-steroidal thioethers.