439595-86-5

Basic information

• Product Name: 2,3,4,6-tetra-O-acetyl-1-N-phenyl acetyl-β-D-glucopyranosylamine
• Synonyms: 2,3,4,6-tetra-O-acetyl-1-N-phenyl acetyl-β-D-glucopyranosylamine
• CAS NO: 439595-86-5
• Molecular Weight: 465.457
• Mol File: 439595-86-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,3,4,6-tetra-O-acetyl-1-N-phenyl acetyl-β-D-glucopyranosylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,6-tetra-O-acetyl-1-N-phenyl acetyl-β-D-glucopyranosylamine(439595-86-5)
• EPA Substance Registry System: 2,3,4,6-tetra-O-acetyl-1-N-phenyl acetyl-β-D-glucopyranosylamine(439595-86-5)

Safety Data

• Hazardous Substances Data: 439595-86-5(Hazardous Substances Data)

Upstream product

• 525589-11-1 2-methyl-4,5-dihydro-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyrano)[2,1-d]-2-oxazoline 
• 13992-25-1 1-azido-1-deoxy-β-D-glucopyranoside tetraacetate 
• 103-80-0 phenylacetyl chloride 
• 20379-61-7 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl azide 
• 103-82-2 phenylacetic acid 
• 23776-85-4 N-(phenylacetyl)oxysuccinimide 
• 61049-78-3 S-pyridin-2-yl 2-phenylethanethioate 

Relevant articles and documents

Stereoselective synthesis of α- and β-glycosylamide derivatives from glycopyranosyl azides via isoxazoline intermediates

Treatment of 2-acetoxy glycopyranosyl azides with Ph3P gave isoxazolines by ring closure of the phosphorimine. Coupling of in situ generated isoxazolines with acylating reagents gave mixtures of α- or β-glycopyranosyl amides. The α/β ratio depe

Synthesis of N-(β-D-glucopyranosyl)- and N-(2-acetamido-2-deoxy- β-D-glucopyranosyl) amides as inhibitors of glycogen phosphorylase

2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl- and 2-acetamido-3,4,6-tri- O-acetyl-2-deoxy-β-D-glucopyranosyl azides were transformed into the corresponding per-O-acetylated N-(β-D-glycopyranosyl) amides via a PMe 3 mediated Staudinger protocol (ge