322479-13-0

Basic information

• Product Name: ethyl (2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
• Synonyms: ethyl (2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside
• CAS NO: 322479-13-0
• Molecular Weight: 912.024
• Mol File: 322479-13-0.mol

Chemical Properties

• CAS DataBase Reference: ethyl (2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside(322479-13-0)
• EPA Substance Registry System: ethyl (2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside(322479-13-0)

Safety Data

• Hazardous Substances Data: 322479-13-0(Hazardous Substances Data)

Upstream product

• 34339-69-0 2,4,6-tri-O-acetyl-3-O-benzyl-α-D-glucopyranosyl bromide 
• 115533-35-2 ethyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 

Downstream Products

• 322479-14-1 2-[(2S,3R,4R,5S,6R)-4-Benzyloxy-5-((2S,3R,4S,5R,6R)-4-benzyloxy-3,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-6-benzyloxymethyl-2-ethylsulfanyl-tetrahydro-pyran-3-yl]-isoindole-1,3-dione 
• 322479-10-7 ethyl (3-O-benzyl-4,6-O-isopropylidene-β-D-arabino-hexopyranosyl-2-ulose)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 322479-15-2 ethyl (3-O-benzyl-4,6-O-isopropylidene-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 

Relevant articles and documents

New factors governing stereoselectivity in borohydride reductions of β-D-glycoside-2-uloses - The peculiar effect of 'activated' DMSO

Comparative evaluation of the manno/gluco ratios obtained in the conventional reductions of β-D-glucoside-2-uloses (1-4, 13 and 14) reveals the influence of the substitution pattern: the presence of a 4,6-O-acetal function results in lower stereoselectivi