1038507-72-0

Basic information

• Product Name: 1,3,4,6-tetra-O-benzyl-β-D-fructofuranosyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-α-D-glucopyranoside
• Synonyms: 1,3,4,6-tetra-O-benzyl-β-D-fructofuranosyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-α-D-glucopyranoside
• CAS NO: 1038507-72-0
• Molecular Weight: 1495.81
• Mol File: 1038507-72-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,3,4,6-tetra-O-benzyl-β-D-fructofuranosyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4,6-tetra-O-benzyl-β-D-fructofuranosyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-α-D-glucopyranoside(1038507-72-0)
• EPA Substance Registry System: 1,3,4,6-tetra-O-benzyl-β-D-fructofuranosyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-α-D-glucopyranoside(1038507-72-0)

Safety Data

• Hazardous Substances Data: 1038507-72-0(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 512-69-6 D-raffinose 

Downstream Products

• 1038507-81-1 2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl-(1→6)-2,3,4-tri-O-benzyl-α-D-glucopyranose 
• 28697-72-5 1,3,4,6-tetra-O-benzyl-α,β-D-fructofuranose 
• 1206803-53-3 1,3,4-tri-O-benzyl-6-O-triethyl-silyl-β-D-fructofuranosyl 2,3,4-tri-O-benzyl-6-O-(2,3,4-tri-O-benzyl-6-O-triethyl-silyl-α-D-galactopyranosyl)-α-D-glucopyranoside 

Relevant articles and documents

Preparation of partially benzylated mono-, di-, and trisaccharides by selective cleavage of the β-fructofuranosidic linkage in fully benzylated sucrose and sucrose-related oligosaccharides under acidic conditions

Several partially benzylated mono-, di-, and trisaccharides having an anomeric hydroxyl group were successfully prepared by selective cleavage of the β-fructofuranosidic linkage in fully benzylated sucrose and sucrose-related oligosaccharides derived from lactosucrose, raffinose, melezitose, stachyose, and nystose under acidic conditions using 1:10 75% aqueous sulfuric acid-dioxane at room temperature for 1 h.