6207-47-2

Basic information

• Product Name: allyl 6-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside
• CAS NO: 6207-47-2
• Molecular Weight: 350.412
• Mol File: 6207-47-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: allyl 6-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 6-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside(6207-47-2)
• EPA Substance Registry System: allyl 6-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside(6207-47-2)

Safety Data

• Hazardous Substances Data: 6207-47-2(Hazardous Substances Data)

Upstream product

• 6207-46-1 allyl 6-O-benzyl-α-D-galactopyranoside 
• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 74494-01-2 (2R,3R,4S,5R,6S)-6-Allyloxy-2-benzyloxymethyl-5-(3-methyl-but-2-enyloxy)-tetrahydro-pyran-3,4-diol 
• 74493-99-5 allyl 3,4,6-tri-O-benzyl-2-O-(3-methylbut-2-enyl)-α-D-galactopyranoside 
• 74524-17-7 cis-prop-1-enyl 3,4,6-tri-O-benzyl-O-α-D-galactopyranoside 
• 74524-16-6 trans-prop-1-enyl 3,4,6-tri-O-benzyl-O-α-D-galactopyranoside 
• 78878-53-2 propyl 2-acetamido-4,6-di-O-benzyl-2-deoxy-3-O-(2,4-di-O-benzoyl-3,6-di-O-benzyl-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 78878-41-8 2,4-di-O-benzoyl-3,6-di-O-benzyl-1-O-p-nitrobenzoyl-α-D-galactopyranose 
• 78878-39-4 allyl 2,4-di-O-benzoyl-3,6-di-O-benzyl-α-D-galactopyranoside 
• 78878-38-3 1-propenyl 2,4-di-O-benzoyl-3,6-di-O-benzyl-α-D-galactopyranoside 
• 78878-48-5 1-propenyl 2-O-benzoyl-3,6-di-O-benzyl-4-O-(tetrahydro-2-pyranyl)-α-D-galactopyranoside 
• 78894-82-3 2,4-di-O-benzoyl-3,6-di-O-benzyl-α-D-galactopyranosyl bromide 
• 78894-84-5 2,4-di-O-benzoyl-3,6-di-O-benzyl-α-D-galactopyranosyl chloride 
• 78878-45-2 1-propenyl 2-O-benzoyl-3,6-di-O-benzyl-4-O-tert-butyldimethylsilyl-α-D-galactopyranoside 
• 78878-52-1 2-O-benzoyl-3,6-di-O-benzyl-4-O-(tetrahydro-2-pyranyl)-α-D-galactopyranosyl chloride 
• 78878-44-1 1-propenyl 4-O-allyl-2-O-benzoyl-3,6-di-O-benzyl-α-D-galactopyranoside 

Relevant articles and documents

Diastereoselective Bromination of Allyl Glycosides Using Tetrabutylammonium Tribromide

Both (R) and (S)-2,3-dibromo-1-propanol with e.e. up to 60percent have been obtained by diastereoselective addition of Br2 to allyl glucosides and galactosides having only one unprotected hydroxyl group at C-2 or C-6 using tetrabutylammonium tribromide, followed by hydrolysis.The absolute configuration is shown to depend on the position of the free hydroxyl and on the configuration at the anomeric centre.