149117-53-3

Basic information

• Product Name: 1,3,4,6-tetra-O-acetyl-2-deoxy-2-<3-(4-tolylureido)>-α-D-glucopyranose
• Synonyms: 1,3,4,6-tetra-O-acetyl-2-deoxy-2-<3-(4-tolylureido)>-α-D-glucopyranose
• CAS NO: 149117-53-3
• Molecular Weight: 480.472
• Mol File: 149117-53-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3,4,6-tetra-O-acetyl-2-deoxy-2-<3-(4-tolylureido)>-α-D-glucopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4,6-tetra-O-acetyl-2-deoxy-2-<3-(4-tolylureido)>-α-D-glucopyranose(149117-53-3)
• EPA Substance Registry System: 1,3,4,6-tetra-O-acetyl-2-deoxy-2-<3-(4-tolylureido)>-α-D-glucopyranose(149117-53-3)

Safety Data

• Hazardous Substances Data: 149117-53-3(Hazardous Substances Data)

Upstream product

• 866416-46-8 1,3,4,6-tetra-O-acetyl-2-deoxy-2-isocyanato-α-D-glucopyranose 
• 106-49-0 p-toluidine 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 103637-78-1 1,3,4,6-tetra-O-acetyl-2-amino-2-deoxy-α-D-glucopyranose hydrobromide 
• 108-24-7 acetic anhydride 
• 622-58-2 p-Tolylisocyanate 
• 14131-62-5 D-glucosamine hydrochloride 
• 22435-64-9 2,3,4,6-tetra-O-acetyl-N-(2,2-diethoxycarbonylvinyl)-β-D-glucopyranosylamine 
• 866416-47-9 N-(p-methylphenyl)-N'-(1,3,4,6-tetra-O-acetyl-2-deoxy-α-D-glucopyranos-2-yl)thiourea 
• 109947-42-4 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-isothiocyanato-α-D-glucopyranose 
• 108967-42-6 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosylamine hydrobromide 

Downstream Products

• 149117-44-2 2-deoxy-2-<3-(4-tolylureido)>-α-D-glucopyranose 

Relevant articles and documents

New synthetic approaches to sugar ureas. Access to ureido-β- cyclodextrins

An efficient method for the preparation of urea-bridged cyclodextrins using triphosgene in the isocyanation step in an aqueous two-phase system is reported. Per-O-acetylated glycopyranosylamines and 2-amino-2-deoxy-α and β-d-glucose were also transformed

THE REACTION OF 2-AMINO-2-DEOXYHEXOPYRANOSES WITH ISOCYANATES. SYNTHESIS OF UREAS AND THEIR TRANSFORMATION INTO HETEROCYCLIC DERIVATIVES.

The reactions of 2-amino-2-deoxyglycopyranoses with aryl isocyanates have been investigated in detail and ureas and heterocyclic derivatives are obtained.The mechanism of formation of glycofuranoimidazolidin-2-ones 62 has now become visible, while