100221-42-9

Basic information

• Product Name: Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-(benzyloxycarbonyl-methyl-amino)-6-methoxy-tetrahydro-pyran-4-yl ester
• CAS NO: 100221-42-9
• Molecular Weight: 467.473
• Mol File: 100221-42-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-(benzyloxycarbonyl-methyl-amino)-6-methoxy-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-(benzyloxycarbonyl-methyl-amino)-6-methoxy-tetrahydro-pyran-4-yl ester(100221-42-9)
• EPA Substance Registry System: Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-(benzyloxycarbonyl-methyl-amino)-6-methoxy-tetrahydro-pyran-4-yl ester(100221-42-9)

Safety Data

• Hazardous Substances Data: 100221-42-9(Hazardous Substances Data)

Upstream product

• 82916-19-6 methyl 2-N-(benzyloxycarbonyl)amino-2-deoxy-α-D-galactopyranoside 
• 501-53-1 benzyl chloroformate 
• 57173-08-7 methyl 2-amino-2-deoxy-α-D-galactopyranoside 
• 82877-95-0 methyl 3,4,6-tri-O-acetyl-2-benzyloxycarbonylamino-2-deoxy-α-D-galactopyranoside 
• 74-88-4 methyl iodide 

Downstream Products

• 100221-43-0 methyl 2-benzyloxycarbonyl(methyl)amino-2-deoxy-α-D-galactopyranoside 

Relevant articles and documents

2-Substituted methyl alpha-D-galactopyranosides: synthesis and binding affinity for the A and B subunits of the Griffonia simplicifolia I isolectins.

The binding affinities of the N-acetyl, N-trifluoroacetyl, N-propionyl, N-formyl, N-benzoyl, N-p-nitrobenzoyl, N-p-aminobenzoyl, and N-methyl derivatives of methyl 2-amino-2-deoxy-alpha-D-galactopyranoside and the 2-O-acetyl, -benzoyl, -benzyl, and -methyl derivatives of methyl alpha-D-galactopyranoside for the A and B subunits of the Griffonia simplicifolia I isolectins have been determined by hapten inhibition analysis of a galactomannan-isolectin precipitation system. Models for these carbohydrate-protein interactions are presented together with an interpretation of the results on the basis of electronic and steric effects.