1352299-64-9

Basic information

• Product Name: (3S,4S,6S)-2-(Acetoxymethyl)-6-((3R,4S,6R)-4,5-diacetoxy-2-(acetoxymethyl)-6-(3-(5-(2-(benzyloxy)-2-oxoethyl)-3-tert-butyl-2,4-dioxoimidazolidin-1-yl)propoxy)tetrahydro-2H-pyran-3-yloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
• CAS NO: 1352299-64-9
• Molecular Weight: 980.972
• Mol File: 1352299-64-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3S,4S,6S)-2-(Acetoxymethyl)-6-((3R,4S,6R)-4,5-diacetoxy-2-(acetoxymethyl)-6-(3-(5-(2-(benzyloxy)-2-oxoethyl)-3-tert-butyl-2,4-dioxoimidazolidin-1-yl)propoxy)tetrahydro-2H-pyran-3-yloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4S,6S)-2-(Acetoxymethyl)-6-((3R,4S,6R)-4,5-diacetoxy-2-(acetoxymethyl)-6-(3-(5-(2-(benzyloxy)-2-oxoethyl)-3-tert-butyl-2,4-dioxoimidazolidin-1-yl)propoxy)tetrahydro-2H-pyran-3-yloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate(1352299-64-9)
• EPA Substance Registry System: (3S,4S,6S)-2-(Acetoxymethyl)-6-((3R,4S,6R)-4,5-diacetoxy-2-(acetoxymethyl)-6-(3-(5-(2-(benzyloxy)-2-oxoethyl)-3-tert-butyl-2,4-dioxoimidazolidin-1-yl)propoxy)tetrahydro-2H-pyran-3-yloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate(1352299-64-9)

Safety Data

• Hazardous Substances Data: 1352299-64-9(Hazardous Substances Data)

Upstream product

• 18464-08-9 2,3,6,2',3',4',6'-hepta-O-acetyl-lactose 
• 13474-68-5 Benzyl fumarate 
• 5160-10-1 2,3,6-tetra-O-acetyl-4-O-(2',3',4',6'-tetra-O-acetyl-β-D-galactopyranosyl)-D-glucopyranosylbromide 
• 92052-38-5 O-<2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-α,β-D-glucopyranosyl>trichloroacetimidate 
• 338744-56-2 3-azidopropyl (2,3,4,6-tetra-O-acetyl-β-O-D-galactopyranosyl)-(1→4)-O-2,3,6-tri-O-acetyl-β-D-glucopyranoside 
• 5965-66-2 LACTOSE 

Downstream Products

• 1352299-34-3 C₅₁H₇₁N₃O₂₃ 

Relevant articles and documents

Three-component, one-pot sequential synthesis of glyco-hydantoin conjugates

The development of new methods for linking sugars to heterocycles and peptides is an attractive area of research because glyco-conjugates play important roles in biology and medicine and are indispensable tools for probing several processes. Herein we report a one-pot, three-component sequential procedure for the synthesis of a novel class of glyco-conjugates, i.e. glyco-hydantoin conjugates, in high yields and very mild conditions, using readily accessible starting materials. We also demonstrated that some of the glyco-hydantoin conjugates obtained are synthons for the preparation of a novel class of glyco-pseudopeptides in which the amino acid is tethered to the sugar through the hydantoin ring. The Royal Society of Chemistry 2011.