114772-89-3

Basic information

• Product Name: 2-butyl-4-chloro-1-[4-(2-carbomethoxyphenoxy)benzyl]-5-hydroxymethylimidazole
• Synonyms: 2-butyl-4-chloro-1-[4-(2-carbomethoxyphenoxy)benzyl]-5-hydroxymethylimidazole
• CAS NO: 114772-89-3
• Molecular Weight: 428.915
• Mol File: 114772-89-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-butyl-4-chloro-1-[4-(2-carbomethoxyphenoxy)benzyl]-5-hydroxymethylimidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-butyl-4-chloro-1-[4-(2-carbomethoxyphenoxy)benzyl]-5-hydroxymethylimidazole(114772-89-3)
• EPA Substance Registry System: 2-butyl-4-chloro-1-[4-(2-carbomethoxyphenoxy)benzyl]-5-hydroxymethylimidazole(114772-89-3)

Safety Data

• Hazardous Substances Data: 114772-89-3(Hazardous Substances Data)

Upstream product

• 30087-38-8 methyl 2-[4-(bromomethyl)phenoxy]benzoate 
• 118-91-2 ortho-chlorobenzoic acid 
• 21905-72-6 methyl 2-(4-methylphenoxy)benzoate 
• 21905-69-1 2-(4-methylphenoxy)-benzoic acid 
• 106-44-5 p-cresol 
• 79047-41-9 2-n-butyl-4-chloro-5-hydroxymethylimidazole 

Downstream Products

• 114822-97-8 2-butyl-1-<4-(2-carboxyphenoxy)benzyl>-4-chloro-5-(hydroxymethyl)imidazole 

Relevant articles and documents

ANGIOTENSIN II RECEPTOR BLOCKING IMIDAZOLES

Substituted imidazoles such as STR1 are useful as angiotensin II blockers. These compounds have activity in treating hypertension and congestive heart failure.

Nonpeptide Angiotensin II Receptor Antagonist: N-imidazoles and Related Compounds as Potent Antihypertensives

A series of compounds has been synthesized and demonstrated to be antagonists of the angiotensin II (AII) receptor.These compounds are structurally related to the N-(benzamidobenzyl)imidazoles and extend the scope of this new class of nonpeptide AII antag