117253-25-5

Basic information

• Product Name: 2-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside
• Synonyms: 2-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside
• CAS NO: 117253-25-5
• Molecular Weight: 981.268
• Mol File: 117253-25-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside(117253-25-5)
• EPA Substance Registry System: 2-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside(117253-25-5)

Safety Data

• Hazardous Substances Data: 117253-25-5(Hazardous Substances Data)

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 4753-07-5 2,3,6,2',3',4',6'-hepta-O-acetyl-lactosyl bromide 
• 103082-77-5 2-(trimethylsilyl)ethyl 2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 2916-68-9 2-(Trimethylsilyl)ethanol 
• 115969-51-2 2-(trimethylsilyl)ethyl O-(β-D-galactopyranosyl)-(1->4)-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 117253-23-3 2-(trimethylsilyl)ethyl 4-O-(4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside 

Downstream Products

• 164525-86-4 2-(trimethylsilyl)ethyl <2,3-bis-O-(phenylmethyl)-β-D-galactopyranosyl>-(1,4)-2,3,6-tris-O-(phenylmethyl)-β-D-glucopyranoside 
• 117253-26-6 2-(trimethylsilyl)ethyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 

Relevant articles and documents

A facile preparation of the methyl 2-tioglycoside of N-glycolylneuraminic acid, an efficient donor of NeuGc

The methyl 2-thioglycoside of N-glycolylneuraminic acid (SMe-NeuGc, 1), which is an efficient donor of NeuGc in the preparation of sialosyl glycoconjugates, was synthesized from N-acetylneuraminic acid (NeuAc) in 6 steps in good yield. 1 could be glycosyl