88510-14-9

Basic information

• Product Name: benzyl 2,3,4-tri-O-acetyl-6-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-β-D-glucopyranoside
• Synonyms: benzyl 2,3,4-tri-O-acetyl-6-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-β-D-glucopyranoside
• CAS NO: 88510-14-9
• Molecular Weight: 668.649
• Mol File: 88510-14-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: benzyl 2,3,4-tri-O-acetyl-6-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2,3,4-tri-O-acetyl-6-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-β-D-glucopyranoside(88510-14-9)
• EPA Substance Registry System: benzyl 2,3,4-tri-O-acetyl-6-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-β-D-glucopyranoside(88510-14-9)

Safety Data

• Hazardous Substances Data: 88510-14-9(Hazardous Substances Data)

Upstream product

• 5239-09-8 Neryl 2,3,4-tri-O-acetyl-6-O-(2,3,4-tri-O-acetyl-6-O-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside 
• 131283-99-3 2,3,4-tri-O-acetyl-6-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-D-glucopyranose 
• 30021-94-4 1,2,3,4-O-tetraacetyl-α-L-rhamnopyranose 
• 100-51-6 benzyl alcohol 
• 4304-12-5 (2R,3R,4S,5S,6R)-2-(benzyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol 
• 868843-87-2 benzyl 6-O-tertbutyldimethylsilyl-β-D-glucopyranoside 
• 125520-01-6 ethyl 2,3,4-tri-O-acetyl-1-thio-α-L-rhamnopyranoside 
• 29868-41-5 benzyl 2,3,4-tri-O-acetyl-β-D-glucopyranoside 
• 127243-74-7 2,3,4-tri-O-acetyl-6-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-D-glucopyranosyl trichloracetamide 
• 374789-78-3 benzyl 2,3,4-tri-O-acetyl-6-O-tertbutyldimethylsilyl-β-D-glucopyranoside 
• 50-99-7 D-glucose 

Downstream Products

• 88510-10-5 1′-O-benzyl-α-L-rhamnopyranosyl-(1″→6′)-β-D-glucopyranoside 

Relevant articles and documents

Chemoenzymatic synthesis of naturally occurring benzyl 6-O-glycosyl-β- D-glucopyranosides

Direct β-glucosidation between benzyl alcohol and D-glucose (5) using the immobilized β-glucosidase from almonds with the synthetic prepolymer ENTP-4000 gave a benzyl β-D-glucoside (1) in 53% yield. The coupling of the benzyl β-D-glucopyranoside congener