161765-88-4

Basic information

• Product Name: ETHYL 2-O-BENZOYL-4,6-O-BENZYLIDENE-BETA-D-GALACTOPYRANOSIDE
• Synonyms: ETHYL 2-O-BENZOYL-4,6-O-BENZYLIDENE-BETA-D-GALACTOPYRANOSIDE;Ethyl 2-O-benzoyl-4,6-O-benzylidene-b-D-galactopyranoside
• CAS NO: 161765-88-4
• Molecular Formula: C₂₂H₂₄O₇
• Molecular Weight: 400.42
• Mol File: 161765-88-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 570.0±50.0 °C(Predicted)
• Appearance: /
• Density: 1.31±0.1 g/cm3(Predicted)
• PKA: 12.41±0.70(Predicted)
• CAS DataBase Reference: ETHYL 2-O-BENZOYL-4,6-O-BENZYLIDENE-BETA-D-GALACTOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 2-O-BENZOYL-4,6-O-BENZYLIDENE-BETA-D-GALACTOPYRANOSIDE(161765-88-4)
• EPA Substance Registry System: ETHYL 2-O-BENZOYL-4,6-O-BENZYLIDENE-BETA-D-GALACTOPYRANOSIDE(161765-88-4)

Safety Data

• Hazardous Substances Data: 161765-88-4(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 541-88-8 Chloroacetic anhydride 

Downstream Products

• 161765-90-8 Ethyl 4,6-O-benzylidene-2-O-benzoyl-3-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-β-D-galactopyranoside 

Relevant articles and documents

Preparation of sialyl Lex analogs as inhibitors of cellular adhesion.

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Sialyl Lex analogues as inhibitors of cellular adhesion

The inventive compounds are analogues of sialyl Lex that inhibit cellular adhesion between a selectin and cells that express sialyl Lex on their surfaces, and their synthetic intermediates. An inventive compound has structure A, STR1

Bivalent sialyl X saccharides

The present invention relates to bivalent sialyl Lewis X saccharide compounds that inhibit cellular binding to a selectin receptor. Pharmaceutical compositions containing a compound of Formula I, and processes for making and using the same are disclosed.