219564-51-9

Basic information

• Product Name: 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetylamino-α-D-glucopyranosyl dibenzyl phosphate
• Synonyms: 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetylamino-α-D-glucopyranosyl dibenzyl phosphate
• CAS NO: 219564-51-9
• Molecular Weight: 661.523
• Mol File: 219564-51-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetylamino-α-D-glucopyranosyl dibenzyl phosphate(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetylamino-α-D-glucopyranosyl dibenzyl phosphate(219564-51-9)
• EPA Substance Registry System: 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetylamino-α-D-glucopyranosyl dibenzyl phosphate(219564-51-9)

Safety Data

• Hazardous Substances Data: 219564-51-9(Hazardous Substances Data)

Upstream product

• 538-37-4 dibenzyl phosphochloridate 
• 212137-44-5 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetamido-α-D-glucopyranose 
• 137766-83-7 2-deoxy-2-trifluoroacetamido-1,3,4,6-tetra-O-acetyl-α,β-D-glucopyranoside 
• 108549-23-1 Dibenzyl N,N-diisopropylphosphoramidite 
• 28719-30-4 3,4,6-Tri-O-acetyl-2-trifluoracetamino-2-desoxy-D-glucose 
• 667462-08-0 2-trifluoroacetamido-2-deoxy-α,β-D-glucopyranose 
• 6736-63-6 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetamido-α-D-glucospyranosyl bromide 

Downstream Products

• 1109-79-1 uridine 5'-(2-amino-2-deoxy-α-D-glucopyranosyl)-diphosphate 

Relevant articles and documents

Chemoenzymatic synthesis of thio-nod factor intermediates - Enzymatic transfer of glucosamine on thiochitobiose derivatives

The chemoenzymatic syntheses of thioanalogues of nodulation factors in which the nonreducing end glucosamine residue is available for the introduction of the fatty acid moiety at the free NH2 group are reported. We are describing the chemical s

A convenient synthesis of α- and β-D-glucosamine-1-phosphate and derivatives

Derivatives of α- and β-D-glucosamine-1-phosphate and of α-D- galactosamine-1-phosphate, as well as free β-D-glucosamine-1-phosphate, were prepared stereoselectively and in high yield by way of the opening of the 1,2-oxazoline derived from the correspondi