174360-42-0

Basic information

• Product Name: benzyl 2-deoxy-2-phthalimido-6-O-trimethylacetyl-β-D-glucopyranoside
• CAS NO: 174360-42-0
• Molecular Weight: 483.518
• Mol File: 174360-42-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl 2-deoxy-2-phthalimido-6-O-trimethylacetyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2-deoxy-2-phthalimido-6-O-trimethylacetyl-β-D-glucopyranoside(174360-42-0)
• EPA Substance Registry System: benzyl 2-deoxy-2-phthalimido-6-O-trimethylacetyl-β-D-glucopyranoside(174360-42-0)

Safety Data

• Hazardous Substances Data: 174360-42-0(Hazardous Substances Data)

Upstream product

• 3282-30-2 pivaloyl chloride 
• 80035-32-1 benzyl 2-deoxy-2-phthalimido-β-D-glucopyranoside 

Downstream Products

• 176166-29-3 2,2-Dimethyl-propionic acid (2R,3S,4R,5R,6R)-6-benzyloxy-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-triacetoxy-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-2-ylmethyl ester 
• 174360-46-4 benzyl O-(2,6-di-O-acetyl-β-D-galactopyranosyl)-(1<*>4)-3-O-acetyl-2-deoxy-2-phthalimido-6-O-trimethylacetyl-β-D-glucopyranoside 
• 174360-45-3 benzyl O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1<*>4)-2-deoxy-2-phthalimido-6-O-trimethylacetyl-β-D-glucopyranoside 

Relevant articles and documents

Synthesis of precursors for the dimeric 3-O-SO3Na Lewis X and Lewis A structures

Stereoselective syntheses of 3-O-SO3Na-β-Gal-(1 → 4)-β-GlcNAc-(1 → 3)-β-Gal-(1 → 4)GlcNAc-β-OBn (15) and 3-O-SO3Na-β-Gal-(1 → 3)-β-GlcNAc-(1 → 3)-β-Gal-(1 → 3)-β-GlcNAc-(1 → 3)-β-Gal-(1 → 4)-Glc-β-OBn (25) were accomplished through the use of two novel glycosyl donors, namely, ethyl O-(2,6-di-O-acetyl-3,4-O-isopropylidene-β-D-galactopyranosyl)(1 → 4)-3-O-acetyl-2-deoxy-2-phthalimido-1-thio-6-O-trimethylacetyl-β-D-gl ucopyranoside (8) and ethyl O-(2,6-di-O-acetyl-3,4-O-isopropylidene-β-D-galactopyranosyl)-(1 → 3)-4-O-acetyl-2-deoxy-2-phthalimido-1-thio-6-O-trimethylacetyl-β-D-gl ucopyranoside (18).