1316823-37-6

Basic information

• Product Name: p-nitrophenyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->3)-methyl(5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-α-D-glycero-D-galacto-2-nonulopyranoside)onate-(2->6)-2-azido-2-deoxy-α-D-galactopyranoside
• Synonyms: p-nitrophenyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->3)-methyl(5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-α-D-glycero-D-galacto-2-nonulopyranoside)onate-(2->6)-2-azido-2-deoxy-α-D-galactopyranoside
• CAS NO: 1316823-37-6
• Molecular Weight: 1378.27
• Mol File: 1316823-37-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: p-nitrophenyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->3)-methyl(5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-α-D-glycero-D-galacto-2-nonulopyranoside)onate-(2->6)-2-azido-2-deoxy-α-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: p-nitrophenyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->3)-methyl(5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-α-D-glycero-D-galacto-2-nonulopyranoside)onate-(2->6)-2-azido-2-deoxy-α-D-galactopyranoside(1316823-37-6)
• EPA Substance Registry System: p-nitrophenyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->3)-methyl(5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-α-D-glycero-D-galacto-2-nonulopyranoside)onate-(2->6)-2-azido-2-deoxy-α-D-galactopyranoside(1316823-37-6)

Safety Data

• Hazardous Substances Data: 1316823-37-6(Hazardous Substances Data)

Upstream product

• 1316823-21-8 p-nitrophenyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->3)-2-azido-2-deoxy-α-D-galactopyranoside 
• 118977-25-6 methyl (phenyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-galacto-2-nonulopyranoside)onate 

Relevant articles and documents

Synthesis of mucin O-glycan core structures as their p-nitro- and p-aminophenyl glycosides

For the investigation of glycosidases, and for the construction of glycan arrays the p-nitrophenyl- and p-aminophenyl glycosides of mucin O-glycan core structures 1-7 and the 2,6-ST-antigen have been chemically synthesized using d-galactose as a precursor for GalNAc residues. GlcNAc residues have partly been introduced using a 4,6-di-O-benzoyl-2,3-N,O-oxazolidinone-protected donor, which allowed deprotection of the formed di- and tri-saccharides in one step using sodium methoxide.