1381871-16-4

Basic information

• Product Name: 3,4,7-tri-O-benzyl-5-O-((2-naphthyl)methyl)-1-deoxy-1-ethoxysulfonyl-α-D-gluco-hept-2-ulopyranose
• Synonyms: 3,4,7-tri-O-benzyl-5-O-((2-naphthyl)methyl)-1-deoxy-1-ethoxysulfonyl-α-D-gluco-hept-2-ulopyranose
• CAS NO: 1381871-16-4
• Molecular Weight: 712.861
• Mol File: 1381871-16-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,4,7-tri-O-benzyl-5-O-((2-naphthyl)methyl)-1-deoxy-1-ethoxysulfonyl-α-D-gluco-hept-2-ulopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,7-tri-O-benzyl-5-O-((2-naphthyl)methyl)-1-deoxy-1-ethoxysulfonyl-α-D-gluco-hept-2-ulopyranose(1381871-16-4)
• EPA Substance Registry System: 3,4,7-tri-O-benzyl-5-O-((2-naphthyl)methyl)-1-deoxy-1-ethoxysulfonyl-α-D-gluco-hept-2-ulopyranose(1381871-16-4)

Safety Data

• Hazardous Substances Data: 1381871-16-4(Hazardous Substances Data)

Upstream product

• 1381871-15-3 2,3,6-tri-O-benzyl-4-O-((2-naphthyl)methyl)-D-glucono-1,5-lactone 
• 62-50-0 Ethyl methanesulfonate 

Downstream Products

• 1381871-20-0 2,6-anhydro-3,4,7-tri-O-benzyl-5-O-((2-naphthyl)methyl)-1-deoxy-1-ethoxysulfonyl-D-gluco-hept-1-enitol 
• 1381871-26-6 methyl 3,4,7-tri-O-benzyl-5-O-((2-naphthyl)methyl)-1-deoxy-1-ethoxysulfonyl-α-D-gluco-hept-2-ulopyranoside 
• 1381871-27-7 methyl 3,4,7-tri-O-benzyl-5-O-((2-naphthyl)methyl)-1-deoxy-1-ethoxysulfonyl-β-D-gluco-hept-2-ulopyranoside 
• 1381871-17-5 3,4,7-tri-O-benzyl-5-O-((2-naphthyl)methyl)-1-deoxy-1-ethoxysulfonyl-α-D-gluco-hept-2-ulopyranosyl chloride 
• 1381871-18-6 ethyl 3,4,7-tri-O-benzyl-5-O-((2-naphthyl)methyl)-1-deoxy-1-ethoxysulfonyl-2-thio-α-D-gluco-hept-2-ulopyranoside 

Relevant articles and documents

Synthesis of sulfonic acid-containing maltose-type keto-oligosaccharides by an iterative approach

Two different series of (2→5)-α-linked homologous keto-oligosaccharides up to tri- and tetrasaccharide were synthesized by an iterative approach, using 3,4,7-tri-O-benzyl-5-O-(2-naphthyl)methyl-1-deoxy-1- ethoxysulfonyl-α-d-gluco-hept-2-ulopyranosyl chloride as a key building block. An iterative cycle consisted of a glycosylation step followed by selective cleavage of the (2-naphthyl)methyl group.