172875-83-1

Basic information

• Product Name: diethyl 2-propyl-1-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-1H-imidazole-4,5-dicarboxylate
• Synonyms: diethyl 2-propyl-1-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-1H-imidazole-4,5-dicarboxylate
• CAS NO: 172875-83-1
• Molecular Weight: 488.546
• Mol File: 172875-83-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: diethyl 2-propyl-1-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-1H-imidazole-4,5-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl 2-propyl-1-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-1H-imidazole-4,5-dicarboxylate(172875-83-1)
• EPA Substance Registry System: diethyl 2-propyl-1-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-1H-imidazole-4,5-dicarboxylate(172875-83-1)

Safety Data

• Hazardous Substances Data: 172875-83-1(Hazardous Substances Data)

Upstream product

• 51802-42-7 2-propylimidazole-4,5-dicarbonitrile 
• 58954-23-7 2-propyl-1H-imidazole-4,5-dicarboxylic acid 
• 172875-56-8 2-Propyl-1-[2'-(2-trityl-2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1H-imidazole-4,5-dicarboxylic acid diethyl ester 

Downstream Products

• 144689-23-6 ethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl}-1H-imidazole-5-carboxylate 

Relevant articles and documents

Nonpeptide angiotensin II receptor antagonists: Synthesis, biological activities, and structure - Activity relationships of imidazole-5-carboxylic acids bearing alkyl, alkenyl, and hydroxyalkyl substituents at the 4-position and their related compounds

A series of imidazole-5-carboxylic acids bearing alkyl, alkenyl, and hydroxyalkyl substituents at the 4-position and their related compounds were prepared and evaluated for their antagonistic activities to the angiotensin II (AII) receptor. Among them, the 4-(1-hydroxyalkyl)-imidazole derivatives had strong binding affinity to the AII receptor and potently inhibited the AII-induced pressor response by intravenous administration. Various esters of these acids showed potent and long-lasting antagonistic activity by oral administration. The most promising compounds were (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl (CS-866) and (pivaloyloxy)-methyl esters of 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[(2′-1H-tetrazol-5-ylbiphenyl-4-yl) -methyl]imidazole-5-carboxylic acid (26c). A study involving stereochemical comparison of 26c with the acetylated C-terminal pentapeptide of AII was also undertaken.