72366-52-0

Basic information

• Product Name: 4-phenyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside
• Synonyms: 4-phenyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside
• CAS NO: 72366-52-0
• Molecular Weight: 616.754
• Mol File: 72366-52-0.mol
• Article Data: 25

Chemical Properties

• CAS DataBase Reference: 4-phenyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(72366-52-0)
• EPA Substance Registry System: 4-phenyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(72366-52-0)

Safety Data

• Hazardous Substances Data: 72366-52-0(Hazardous Substances Data)

Upstream product

• 139212-74-1 N-sodio-N'-(2,3,4,6-tetra-O-benzyl-D-glucopyranosylidene)-4-toluenesulfonohydrazidate 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 108-95-2 phenol 
• 138963-18-5 N'-(2,3,4,6-tetra-O-benzyl-D-glucopyranosylidene)-4-toluenesulfonohydrazide 
• 138963-17-4 N'-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-4-toluenesulfonohydrazide 
• 53008-62-1 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl iodide 
• 4132-28-9 2,3,4,6-tetra-O-benzyl-D-mannopyranose 
• 92470-93-4 (2R,3R,4S,5S,6R)-3,4,5-tris(benzyloxy)-2-((benzyloxy)methyl)-6-chlorotetrahydro-2H-pyran 
• 3262-89-3 triphenylboroxine 
• 126786-18-3 1-azi-2,3,4,6-tetra-O-benzyl-1-deoxy-D-mannopyranose 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 74808-09-6 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate 
• 194088-19-2 (2R,3R,4S,5R,6S)-3,4,5-tris(benzyloxy)-2-(benzyloxymethyl)-6-(prop-2-ynyloxy)tetrahydro-2H-pyran 
• 98-80-6 phenylboronic acid 

Downstream Products

• 1464-44-4 phenyl-β-D-glucopyranoside 
• 84799-77-9 methyl 2,3,4,6-tetra-O-benzyl-D-glucopyranoside 

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.