28542-03-2

Basic information

• Product Name: methyl 6-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside
• Synonyms: methyl 6-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside
• CAS NO: 28542-03-2
• Molecular Weight: 324.374
• Mol File: 28542-03-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 6-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 6-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside(28542-03-2)
• EPA Substance Registry System: methyl 6-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside(28542-03-2)

Safety Data

• Hazardous Substances Data: 28542-03-2(Hazardous Substances Data)

Upstream product

• 23392-30-5 methyl 6-O-benzyl-α-D-galactopyranoside 
• 67-64-1 acetone 
• 100-39-0 benzyl bromide 
• 40269-01-0 methyl 3,4-O-isopropylidene-α-D-galactopyranoside 
• 620-05-3 iodomethylbenzene 
• 4064-06-6 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 59-23-4 D-Galactose 
• 35526-05-7 6-O-benzyl-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 100-52-7 benzaldehyde 
• 87817-81-0 (3aS,4R,6S,7R,7aS)-6-Methoxy-2,2-dimethyl-7-trimethylsilanyloxy-4-trimethylsilanyloxymethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran 

Downstream Products

• 94715-30-7 2-O-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)-6-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside 
• 94715-31-8 methyl 6-O-benzyl-2-O-(β-D-xylopyranosyl)-α-D-galactopyranoside 
• 53008-63-2 methyl 2,6-di-O-benzyl-3,4-bis(O-(p-bromobenzoyl))-α-D-galactopyranoside 
• 80326-17-6 methyl 3,4-bis(O-(p-bromobenzoyl))-α-D-galactopyranoside 
• 53685-11-3 (2R,3R,4S,5R,6S)-5-Benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3,4-diol 
• 53685-10-2 methyl 2,6-di-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside 

Relevant articles and documents

Synthesis of biologically potent α1 →2-linked disaccharide derivatives via regioselective one-pot protection - Glycosylation

A highly regioselective benzyl and allyl protection of D-hexopyranosides allows their application in the synthesis of biologically potent α1→2 linked disaccharide derivatives by means of a regioselective one-pot protection-glycosylation (see scheme).

Selective benzylation of some D-galactopyranosides

-