209005-11-8

Basic information

• Product Name: dibenzyl (3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranosyl)phosphate
• Synonyms: dibenzyl (3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranosyl)phosphate
• CAS NO: 209005-11-8
• Molecular Weight: 568.49
• Mol File: 209005-11-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: dibenzyl (3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranosyl)phosphate(CAS DataBase Reference)
• NIST Chemistry Reference: dibenzyl (3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranosyl)phosphate(209005-11-8)
• EPA Substance Registry System: dibenzyl (3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranosyl)phosphate(209005-11-8)

Safety Data

• Hazardous Substances Data: 209005-11-8(Hazardous Substances Data)

Upstream product

• 1623-08-1 phosphoric acid dibenzyl ester 
• 801291-55-4 3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranosyl bromide 
• 141395-49-5 [(2R,3R,4S,5S)-3,4,6-triacetoxy-5-fluoro-tetrahydropyran-2-yl]methyl acetate 
• 2873-29-2 D-glucal triacetate 
• 75788-45-3 3,4,6-tri-O-acetyl-2-deoxy-α-D-arabino-hexopyranosyl bromide 
• 226382-72-5 3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranose 
• 108549-23-1 Dibenzyl N,N-diisopropylphosphoramidite 
• 7226-42-8 1,3,4,6-tetra-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranoside 
• 69515-91-9 1,3,4,6-tetra-O-acetyl-2-deoxy-D-glucopyranose 
• 61-58-5 2-deoxy-D-arabino-hexopyranose 

Downstream Products

• 1590360-16-9 dibenzyl (2-deoxy-2-fluoro-α-D-mannopyranosyl)phosphate 

Relevant articles and documents

Phosphodiesters serve as potentially tunable aglycones for fluoro sugar inactivators of retaining β-glycosidases

2-Deoxy-2-fluoroglycosides bearing dibenzyl phosphate and phosphonate aglycones were synthesised and tested as covalent inactivators of several retaining α- and β-glycosidases. β-d-Gluco-, -manno- and -galacto-configured benzyl-benzylphosphonate derivatives efficiently inactivated β-gluco-, β-manno- and β-galactosidases, while α-gluco- and α-manno-configured phosphate and phosphonate derivatives served instead as slow substrates. This journal is the Partner Organisations 2014.