110900-47-5

Basic information

• Product Name: N-(Benzyloxycarbonyl)-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-(2-azido-4,6-di-O-benzoyl-2-desoxy-β-D-galactopyranosyl)>-L-serin-benzylester
• Synonyms: N-(Benzyloxycarbonyl)-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-(2-azido-4,6-di-O-benzoyl-2-desoxy-β-D-galactopyranosyl)>-L-serin-benzylester
• CAS NO: 110900-47-5
• Molecular Weight: 1055.02
• Mol File: 110900-47-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(Benzyloxycarbonyl)-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-(2-azido-4,6-di-O-benzoyl-2-desoxy-β-D-galactopyranosyl)>-L-serin-benzylester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(Benzyloxycarbonyl)-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-(2-azido-4,6-di-O-benzoyl-2-desoxy-β-D-galactopyranosyl)>-L-serin-benzylester(110900-47-5)
• EPA Substance Registry System: N-(Benzyloxycarbonyl)-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-(2-azido-4,6-di-O-benzoyl-2-desoxy-β-D-galactopyranosyl)>-L-serin-benzylester(110900-47-5)

Safety Data

• Hazardous Substances Data: 110900-47-5(Hazardous Substances Data)

Upstream product

• 110797-27-8 Ethyl-2-azido-4,6-di-O-benzoyl-2-desoxy-1-thio-β-D-galactopyranosid 
• 110797-30-3 Ethyl-3,4,6-tri-O-acetyl-2-azido-2-desoxy-1-thio-β-D-galactopyranosid 
• 110825-39-3 Ethyl-2-azido-2-desoxy-1-thio-β-D-galactopyranosid 
• 68733-05-1 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-galactopyranosyl nitrate 
• 110797-26-7 3,4,6-Tri-O-acetyl-2-azido-2-desoxy-β-D-galactopyranosyl-ethylxanthogenat 
• 613-90-1 benzoyl cyanide 
• 21209-51-8 N-(Benzyloxycarbonyl)-L-serin-benzylester 
• 110797-39-2 Ethyl-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-2-azido-4,6-di-O-benzoyl-2-desoxy-1-thio-β-D-galactopyranosid 

Relevant articles and documents

Building Units of Oligosaccharides, LXXXVI1). - Glycosidation with Thioglycosides of Oligosaccharides to Segments of O-Glycoproteins.

In the presence of dimethyl(methylthio)sulfonium triflate (DMTST) thioglycosides of mono-, di-, tri-, and tetrasaccharides, which contain a 2-azido-2-deoxy-D-galactose as reducing unit, can react with the hydroxy group of selectively blocked derivatives of L-serine.These reactions yield the corresponding O-glycosides.Preferentially the α-glycosidically bound products will be obtained.In this way the trisaccharide glycoside 46 was prepared, which represents the core-II structure of mucins α-glycosidically linked to L-serine.Methyl triflate as promoter of this thioglycosidation is less efficient than DMTST.