82145-23-1

Basic information

• Product Name: 1H-Imidazole-4-carboxamide, 5-(benzoylamino)-
• CAS NO: 82145-23-1
• Molecular Formula: C11H10N4O2
• Molecular Weight: 230.226
• Mol File: 82145-23-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1H-Imidazole-4-carboxamide, 5-(benzoylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole-4-carboxamide, 5-(benzoylamino)-(82145-23-1)
• EPA Substance Registry System: 1H-Imidazole-4-carboxamide, 5-(benzoylamino)-(82145-23-1)

Safety Data

• Hazardous Substances Data: 82145-23-1(Hazardous Substances Data)

Upstream product

• 360-97-4 5-Aminoimidazole-4-carboxamide 
• 98-88-4 benzoyl chloride 

Downstream Products

• 82145-38-8 9-(2-Benzoxyethoxymethyl)-2-phenylhypoxanthine 
• 82145-35-5 7-(2-Benzoxyethoxymethyl)-2-phenylhypoxanthine 
• 82145-40-2 9-(2-Hydroxyethoxymethyl)-2-phenylhypoxanthine 
• 18503-16-7 2-Phenylhypoxanthine 
• 82145-26-4 5-Benzamido-1-(2-benzoyloxyethoxymethyl)-4-carbamoylimidazole 
• 82145-25-3 5-Benzamido-3-(2-benzoyloxyethoxymethyl)-4-carbamoylimidazole 

Relevant articles and documents

SYNTHESIS AND PROPERTIES OF ANALOGS OF 5(4)-AMINOIMIDAZOLE-4(5)-CARBOXAMIDE AND PURINES. ACYLATION OF 5(4)-AMINOIMIDAZOLE DERIVATIVES.

The acylation of 5(4)-aminoimidazole derivatives was studied.It is shown that acylation by means of carboxylic acid anhydrides and chlorides takes place at the amino group, whereas acylation by means of chlorocarbonic acid esters takes place at the nitrogen atoms of the imidazole ring.Methods for the selective introduction of a carbomethoxy group in the 1, 3, and 5 positions of the 5(4)-aminoimidazole-4(5)-carboxamide molecule were developed.