273397-25-4

Basic information

• Product Name: Methyl-4,6-di-O-(4-methoxybenzylidene)-2,3-di-O-benzoyl-α-D-glucopyranoside
• Synonyms: Methyl-4,6-di-O-(4-methoxybenzylidene)-2,3-di-O-benzoyl-α-D-glucopyranoside;Methyl 2,3-di-O-benzoyl-4,6-O-(4-methoxybenzylidene)-a-D-glucopyranoside;Methyl 4,6-O-[(S)-(4-methoxyphenyl)methylene]-alpha-D-galactopyranoside dibenzoate
• CAS NO: 273397-25-4
• Molecular Formula: C₂₉H₂₈O₉
• Molecular Weight: 520.531
• Product Categories: Carbohydrates
• Mol File: 273397-25-4.mol

Chemical Properties

• Boiling Point: 646.1±55.0 °C(Predicted)
• Appearance: /
• Density: 1.33±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Methyl-4,6-di-O-(4-methoxybenzylidene)-2,3-di-O-benzoyl-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl-4,6-di-O-(4-methoxybenzylidene)-2,3-di-O-benzoyl-α-D-glucopyranoside(273397-25-4)
• EPA Substance Registry System: Methyl-4,6-di-O-(4-methoxybenzylidene)-2,3-di-O-benzoyl-α-D-glucopyranoside(273397-25-4)

Safety Data

• Hazardous Substances Data: 273397-25-4(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 185754-26-1 (2S,4aR,7R,8R,8aR)-6-methoxy-2-(4-methoxyphenyl)hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol 
• 93-97-0 benzoic acid anhydride 

Downstream Products

• 273397-26-5 methyl 2,3-di-O-benzoyl-6-O-(4-methoxybenzyl)-α-D-galactopyranoside 
• 294639-18-2 methyl 4-amino-2,3-di-O-benzoyl-4-deoxy-6-O-(4-methoxybenzyl)-α-D-glucopyranoside 
• 294639-16-0 methyl 4-azido-2,3-di-O-benzoyl-4-deoxy-6-O-(4-methoxybenzyl)-α-D-glucopyranoside 
• 294639-14-8 methyl 2,3-di-O-benzoyl-4-O-mesyl-6-O-(4-methoxybenzyl)-α-D-galactopyranoside 

Relevant articles and documents

Regioselective Benzoylation of 4,6-O-Benzylidene Acetals of Glycopyranosides in the Presence of Transition Metals

Benzoylation of 4,6-O-benzylidene acetals of glycopyranosides by benzoic anhydride in acetonitrile in the presence of Cu(CF3COO)2 as a promoter gave 2-benzoates for α-D-glucopyranosides and α-D-mannopyranosides and 3-benzoates for β-D-galactopyranosides in good yields with high regioselectivity. Benzoylation of 4,6-O-benzylidene acetals of glycopyranosides of D-galactose and D-mannose by benzoyl chloride in the presence of MoO2(acac)2 as a catalyst in all studied cases led to regioselective 3-substitution.

Stereocontrolled preparation of 2-,3- and 4-isothiocyanato aldopyranose derivatives

The regio- and stereocontrolled introduction of an isothiocyanato group into the positions 2, 3 and 4 of glycopyranose derivatives starting from glycosides, glycosylamines, and aminosugars is reported. Isothiocyanato sugars with D-gluco, D-allo and D-mann