74741-49-4

Basic information

• Product Name: cyclohexylmethyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside
• Synonyms: cyclohexylmethyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside
• CAS NO: 74741-49-4
• Molecular Weight: 636.829
• Mol File: 74741-49-4.mol
• Article Data: 25

Chemical Properties

• CAS DataBase Reference: cyclohexylmethyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: cyclohexylmethyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside(74741-49-4)
• EPA Substance Registry System: cyclohexylmethyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside(74741-49-4)

Safety Data

• Hazardous Substances Data: 74741-49-4(Hazardous Substances Data)

Upstream product

• 88773-80-2 cyclohexylmethyl trimethylsilyl ether 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 90357-89-4 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl trichloroacetimidate 
• 100-49-2 cyclohexylmethyl alcohol 
• 74808-09-6 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate 
• 132201-75-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose trichloroacetimidate 
• 78153-79-4 2,3,4,6-tetra-O-benzyl-D-glucopyranosyl fluoride 
• 80300-30-7 1-O-acetyl-2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 193953-69-4 2,3,4,6-tetra-O-benzyl-D-glucopyranosyl diethyl phosphite 
• 62774-37-2 phenyl 2,3,4,6-tetra-O-acetyl-1-thio-α-D-glucopyranoside 
• 205518-20-3 Carbonic acid cyclohexylmethyl ester (3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl ester 
• 104992-64-5 methyl 2,3,4,6-tetra-O-benzyl-1-thio-β-D-glucopyranoside 
• 942907-29-1 Imidazole-1-carboxylic acid (3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl ester 
• 82300-58-1 dibezylphosphoryl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside 

Relevant articles and documents

Visible light promoted method for constructing O-glycoside bonds

The invention discloses a visible light promoted method for constructing O-glycoside bonds. Glycosyl trichloroacetimidate is taken as a donor, and phenolic compounds are taken as a photocatalyst; a molecular sieve is added; and the O-glycoside bonds are g

A visible light promoted O-glycosylation with glycosyl trichloroacetimidates using eosin Y as an organo photoacid

A photoacid catalyzed O-glycosylation of alcohols with glycosyl trichloroacetimidates in the presence of commercially available phenolic photoacids, fluorescein, 4′,5′-dibromo-fluorescein, and eosin Y under visible light irradiation by blue LEDs was devel

Photo-induced glycosylation using reusable organophotoacids

The glycosylation reactions of glycosyl trichloroacetimidates and several alcohols using an organophotoacid as an activator under photoirradiation proceeded smoothly to give the corresponding glycosides in high yields. The organophotoacid was recovered and reused without any loss of efficiency. This journal is the Partner Organisations 2014.