77667-56-2

Basic information

• Product Name: 4-phenyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside
• Synonyms: 4-phenyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside
• CAS NO: 77667-56-2
• Molecular Weight: 616.754
• Mol File: 77667-56-2.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: 4-phenyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside(77667-56-2)
• EPA Substance Registry System: 4-phenyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside(77667-56-2)

Safety Data

• Hazardous Substances Data: 77667-56-2(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 4630-62-0 phenyl-α-D-glucopyranoside 
• 89025-46-7 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl fluoride 
• 108-95-2 phenol 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 108-86-1 bromobenzene 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 98-80-6 phenylboronic acid 
• 936326-60-2 phenyl(2,4,6-trimethoxyphenyl)iodonium 4-methylbenzenesulfonate 
• 80300-30-7 1-O-acetyl-2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 126709-11-3 1,5-anhydro-2,3,4,6-tetra-O-benzyl-1-hydrazi-D-glucitol 
• 138963-17-4 N'-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-4-toluenesulfonohydrazide 
• 139212-74-1 N-sodio-N'-(2,3,4,6-tetra-O-benzyl-D-glucopyranosylidene)-4-toluenesulfonohydrazidate 
• 1095-03-0 triphenylborane 

Relevant articles and documents

Stereoselective O-Glycosylations by Pyrylium Salt Organocatalysis**

Despite many years of invention, the field of carbohydrate chemistry remains rather inaccessible to non-specialists, which limits the scientific impact and reach of the discoveries made in the field. Aiming to increase the availability of stereoselective

Stereoselective β-mannosylations and β-rhamnosylations from glycosyl hemiacetals mediated by lithium iodide

Stereoselective β-mannosylation is one of the most challenging problems in the synthesis of oligosaccharides. Herein, a highly selective synthesis of β-mannosides and β-rhamnosides from glycosyl hemi-acetals is reported, following a one-pot chlorination,

Copper-mediated anomeric: O -arylation with organoboron reagents

Copper-mediated couplings of arylboroxines with glycosyl hemiacetals furnish O-aryl glycosides via Csp2-O bond formation. The method enables the anomeric O-arylation of protected pyranose and furanose derivatives, and is tolerant of functionalized arylboroxine partners. Whereas mixtures of anomers are formed from glucopyranose, galactopyranose and arabinofuranose hemiacetals, the α-anomer is generated selectively from mannopyranose and mannofuranose-derived substrates.