77016-11-6

Basic information

• Product Name: benzyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-4-O-(2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranosyl)-α-D-glucopyranoside
• Synonyms: benzyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-4-O-(2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranosyl)-α-D-glucopyranoside
• CAS NO: 77016-11-6
• Molecular Weight: 950.052
• Mol File: 77016-11-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: benzyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-4-O-(2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranosyl)-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-4-O-(2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranosyl)-α-D-glucopyranoside(77016-11-6)
• EPA Substance Registry System: benzyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-4-O-(2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranosyl)-α-D-glucopyranoside(77016-11-6)

Safety Data

• Hazardous Substances Data: 77016-11-6(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 70209-55-1 benzyl 2-acetamido-3,6-di-O-benzyl-4-O-(4,6-O-benzylidene-β-D-galactopyranosyl)-2-deoxy-α-D-glucopyranoside 
• 98-88-4 benzoyl chloride 
• 100-39-0 benzyl bromide 
• 70209-54-0 Benzyl-2-acetamido-3,6-di-O-benzyl-2-desoxy-4-O-(β-D-galactopyranosyl)-α-D-glucopyranosid 
• 55287-49-5 benzyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 14146-27-1 benzyl 3-O-benzyl-2-acetamido-2-deoxy-α-D-glucopyranoside 
• 58700-48-4 Benzyl-2-acetamido-3,6-di-O-benzyl-2-desoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-α-D-glucopyranosid 

Relevant articles and documents

Bausteine von Oligosacchariden, XX. Synthese der Oligosaccharid-Determinanten der Blutgruppensubstanzen der Type 2 des ABH-Systems. Diskussion der &α-Glycosid-Synthese

The antigenic determinants of type 2 of blood-group substances A and B (23 and 24) as well as blood-group substance H (17) were synthesized by selective glycosidation reactions combined with a series of blocking and deblocking steps.The possibilities and optimization of the α-glycoside synthesis are discussed.In hemagglutination inhibition tests the synthetic haptens A and B of type 2 and type 1 show a similar selective inhibitory effect.In case of hapten H, however, great differences can be observed.Here the type 2 exhibited a strong inhibition activity, whereas type 1 only showed an extremly low activity.This leads to the conclusion that in the determinants of the ABH-system on the surface of erythrocytes the chemical structure of type 2 is predominating.