213185-35-4

Basic information

• Product Name: phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-thio-β-D-galactopyranoside
• Synonyms: phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-thio-β-D-galactopyranoside
• CAS NO: 213185-35-4
• Molecular Weight: 662.847
• Mol File: 213185-35-4.mol

Chemical Properties

• CAS DataBase Reference: phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-thio-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-thio-β-D-galactopyranoside(213185-35-4)
• EPA Substance Registry System: phenyl 3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-1-thio-β-D-galactopyranoside(213185-35-4)

Safety Data

• Hazardous Substances Data: 213185-35-4(Hazardous Substances Data)

Upstream product

• 183875-28-7 phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside 
• 77790-46-6 1,2-di-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranose 
• 4551-15-9 phenylthiotrimethylsilane 
• 824-94-2 p-methoxybenzyl chloride 
• 183875-29-8 phenyl 3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside 

Downstream Products

• 213185-39-8 phenyl [3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-α-D-galactopyranosyl]-(1->3)-(2-acetamido-4,6-di-O-acetyl-2-deoxy-α-D-glucopyranosyl)-(1->3)-2-O-benzoyl-4-O-benzyl-1-thio-α-L-rhamnopyranoside 
• 204199-48-4 phenyl (3,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-[4,6-di-O-acetyl-2-deoxy-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranosyl]-(1->3)-2-O-benzoyl-4-O-benzyl-1-thio-α-L-rhamnopyranoside 
• 213185-40-1 phenyl [3,4,6-tri-O-benzyl-α-D-galactopyranosyl]-(1->3)-(2-acetamido-4,6-di-O-acetyl-2-deoxy-α-D-glucopyranosyl)-(1->3)-2-O-benzoyl-4-O-benzyl-1-thio-α-L-rhamnopyranoside 
• 213185-38-7 phenyl [3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-α-D-galactopyranosyl]-(1->3)-(4,6-di-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl)-(1->3)-2-O-benzoyl-4-O-benzyl-1-thio-α-L-rhamnopyranoside 
• 204199-47-3 phenyl [3,4,6-tri-O-benzyl-2-O-(4-methoxybenzyl)-α-D-galactopyranosyl]-(1->3)-(4,6-di-O-acetyl-2-amino-2-deoxy-α-D-glucopyranosyl)-(1->3)-2-O-benzoyl-4-O-benzyl-1-thio-α-L-rhamnopyranoside 
• 904690-83-1 2-(trimethylsilyl)ethyl 3,4,6-tri-O-benzyl-2-O-p-methoxybenzyl-α-D-galactopyranosyl-(1->3)-2-acetamido-4,6-di-O-acetyl-2-deoxy-α-D-glucopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside 
• 904690-82-0 2-(trimethylsilyl)ethyl 3,4,6-tri-O-benzyl-2-O-p-methoxybenzyl-α-D-galactopyranosyl-(1->3)-4,6-di-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside 
• 904690-84-2 2-(trimethylsilyl)ethyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-galactopyranosyl-(1->3)-2-acetamido-4,6-di-O-acetyl-2-deoxy-α-D-glucopyranosyl-(1->3)-2-O-benzoyl-4-O-benzyl-α-L-rhamnopyranoside 
• 904690-81-9 3,4,6-tri-O-benzyl-2-O-p-methoxybenzyl-α,β-D-galactopyranosyl trichloroacetimidate 

Relevant articles and documents

Synthesis of glycoconjugate vaccines against Shigella dysenteriae type 1

Syntheses of hexadecasaccharide and smaller fragments corresponding to one-four repeating units of the O-specific polysaccharide of Shigella dysenteriae type 1 are reported in a reactive aglycon-linked from. Two tetrasaccharide donor/acceptor repeating units were assembled from monosaccharide precursors in a stepwise fashion and used in a linear, iterative manner to construct the higher-membered saccharides using Schmidt's glycosylation technique that proved superior to others tested. Single-point attachment of the saccharides to human serum albumin, using a secondary heterobifunctional spacer, afforded a range of glycoconjugates for a detailed evaluation of their immunological characteristics.