114924-71-9

Basic information

• Product Name: 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(3-phenylureido)-β-D-glucopyranose
• Synonyms: 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(3-phenylureido)-β-D-glucopyranose
• CAS NO: 114924-71-9
• Molecular Weight: 466.445
• Mol File: 114924-71-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(3-phenylureido)-β-D-glucopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(3-phenylureido)-β-D-glucopyranose(114924-71-9)
• EPA Substance Registry System: 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(3-phenylureido)-β-D-glucopyranose(114924-71-9)

Safety Data

• Hazardous Substances Data: 114924-71-9(Hazardous Substances Data)

Upstream product

• 4780-17-0 1,3,4,6-tetra-O-acetyl-2-deoxy-2-isocyanato-β-D-glucopyranose 
• 62-53-3 aniline 
• 103-72-0 phenyl isothiocyanate 
• 90-76-6 2-deoxy-2-amino glucose 
• 103-71-9 phenyl isocyanate 
• 14131-62-5 D-glucosamine hydrochloride 
• 5432-46-2 1,3,4,6-tetra-O-acetyl-D-glucosamine hydrochloride 
• 108-24-7 acetic anhydride 
• 134122-77-3 2-deoxy-2-(3-phenylureido)-D-glucopyranose 

Downstream Products

• 134122-77-3 2-deoxy-2-(3-phenylureido)-β-D-glucopyranose 
• 134122-78-4 2-deoxy-2-(3-phenylureido)-α-D-glucopyranose 
• 149117-58-8 (4R,5R)-4-(D-arabino-tetritol-1-yl)-5-hydroxy-1-phenylimidazolidin-2-one 
• 111239-65-7 methyl 3,4,6-tri-O-acetyl-2-deoxy-2-(3-phenylureido)-β-D-glucopyranoside 
• 76444-17-2 1-phenyl-(1,2-dideoxy-α-D-glucofurano)<2,1-d>imidazolidin-2-one 
• 129694-04-8 2-Phenylamino-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucofurano)<2,1-d>-2-oxazoline 
• 110336-60-2 3,4,6-tri-O-acetyl-2-deoxy-2-(3-phenylureido)-α-D-glucopyranose 
• 111240-35-8 tri-O-acetyl-2-(N'-phenyl-ureido)-2-deoxy-α-D-glucopyranosyl bromide 
• 110336-60-2 O³,O⁴,O⁶-triacetyl-2-(N'-phenyl-ureido)-2-deoxy-β-D-glucopyranose 

Relevant articles and documents

Synthesis of novel glycosyl imidazolidine-2,4,5-trione derivatives

A series of glycosyl imidazolidine-2,4,5-trione derivatives were achieved by condensing per-O-acetylated glucosamine, triphosgene, amines and oxalyl chloride. The convenient and efficient method afforded the desired products with good to excellent yields

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