25018-28-4

Basic information

• Product Name: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside
• Synonyms: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside
• CAS NO: 25018-28-4
• Molecular Weight: 1063.3
• Mol File: 25018-28-4.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(25018-28-4)
• EPA Substance Registry System: 2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(25018-28-4)

Safety Data

• Hazardous Substances Data: 25018-28-4(Hazardous Substances Data)

Upstream product

• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 25320-59-6 tetra-O-benzyl glucopyranosyl chloride 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 4132-28-9 2,3,4,6-tetra-O-benzyl-D-mannopyranose 
• 1370590-24-1 2-allylphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside 
• 1370590-22-9 2-allylphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 83-87-4 D-Mannose pentaacetate 
• 60-12-8 2-phenylethanol 
• 100-39-0 benzyl bromide 
• 881198-66-9 2-allyloxyphenyl 2,3,4,6-tetra-O-benzyl-β-D-mannopyranoside 
• 83462-67-3 methyl 2,3,4,6-tetra-O-benzyl-D-mannopyranoside 
• 53270-14-7 benzyl 2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 187083-12-1 methyl 2,6-dibenzyl-3-methyl-α-D-mannopyranoside 

Downstream Products

• 499-23-0 β,β-trehalose 

Relevant articles and documents

Molecular sieves promote stereocontrolled αα-disaccharide formation via direct dimerization of free sugars

Some commercial molecular sieves promote direct dimerization of free pyranose and furanose sugars stereoselectively into the corresponding α,α-disaccharides.

Formation of O-glycosidic linkages from 1-hydroxy sugars by bismuth(III) triflate-catalyzed dehydrative glycosidation

This paper describes the direct formation of various O-glycosidic linkages from 1-hydroxy sugars by bismuth(III) triflate-catalyzed dehydrative glycosidation. The condensation reactions of 1 -hydroxy sugars with some primary alcohols in the presence of on

Sulfoxide Covalent Catalysis: Application to Glycosidic Bond Formation

A versatile glycosylation reaction is used to establish the process of sulfoxide covalent catalysis. Hemiacetals are activated by benzenesulfonic anhydride and a dialkyl sulfoxide catalyst, nBu2SO, for coupling with various nucleophiles (Nu; se