149117-40-8

Basic information

• Product Name: 2-<3-(4-chlorophenylureido)>-2-deoxy-α-D-glucopyranose
• Synonyms: 2-<3-(4-chlorophenylureido)>-2-deoxy-α-D-glucopyranose
• CAS NO: 149117-40-8
• Molecular Weight: 332.741
• Mol File: 149117-40-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-<3-(4-chlorophenylureido)>-2-deoxy-α-D-glucopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 2-<3-(4-chlorophenylureido)>-2-deoxy-α-D-glucopyranose(149117-40-8)
• EPA Substance Registry System: 2-<3-(4-chlorophenylureido)>-2-deoxy-α-D-glucopyranose(149117-40-8)

Safety Data

• Hazardous Substances Data: 149117-40-8(Hazardous Substances Data)

Upstream product

• 35804-60-5 1,3,4,6-tetra-O-acetyl-2-<3-(4-chlorophenylureido)>-2-deoxy-β-D-glucopyranose 
• 4780-17-0 1,3,4,6-tetra-O-acetyl-2-deoxy-2-isocyanato-β-D-glucopyranose 
• 5432-46-2 1,3,4,6-tetra-O-acetyl-D-glucosamine hydrochloride 
• 104-12-1 p-chlorphenylisocyanate 
• 10034-19-2 1,3,4,6-tetra-O-acetyl-2-amino-2-deoxy-α-D-glucopyranose hydrochloride 
• 14131-62-5 D-glucosamine hydrochloride 
• 129784-21-0 1,3,4,6-Tetra-O-acetyl-2-<3-(4-chlorophenyl)ureido>-2-deoxy-α-D-glucopyranose 

Downstream Products

• 35808-11-8 1-(4-chlorophenyl)-(1,2-dideoxy-α-D-glucofurano)<2,1-d>imidazolidin-2-one 
• 148943-80-0 3,4,6-tri-O-acetyl-2-deoxy-2-<3-(4-chlorophenylureido)>-α-D-glucopyranose 
• 149117-59-9 (4R,5R)-4-(D-arabino-tetritol-1-yl)-1-(4-chlorophenyl)-5-hydroxyimidazolidin-2-one 
• 149038-33-5 (4S,5S)-4-(D-arabino-tetritol-1-yl)-1-(4-chlorophenyl)-5-hydroxyimidazolidin-2-one 
• 129784-21-0 1,3,4,6-Tetra-O-acetyl-2-<3-(4-chlorophenyl)ureido>-2-deoxy-α-D-glucopyranose 
• 35804-60-5 1,3,4,6-tetra-O-acetyl-2-<3-(4-chlorophenylureido)>-2-deoxy-β-D-glucopyranose 

Relevant articles and documents

Synthesis and antifungal activity of d-glucopyranosyl ureas and d-glucofurano-imidazolidine-2-ones

A series of N-β-d-glucopyranosyl-N'-substituted phenyl ureas were synthesized by reaction of glucosyl isocyanate with arylamines and glycosamine with aryl isocyanates, and a series of d-glucofurano-imidazolidine-2-ones were obtained via deacetylation of glycosylureas. Although some of the compounds have already been described, most were prepared for the first time in this work. The structures of all the compounds synthesized were confirmed by IR, 1H NMR, and, in part, by 13C NMR. Antifungal activity of the title compounds was determined against four kinds of plant pathogenic fungi, Sclerotinia sclerotiorum, Fusarium graminearum, Fusarium oxysporum, and Bipolaris maydis. Preliminary bioassay indicates that most of glycosylureas had some activity against S. sclerotiorum; for some, the antifungal activity was strong. However, most of the imidazolidine-2-ones had weak antifungal activity.