114772-96-2

Upstream product

• 6424-25-5 methyl 2-(4-methylbenzoyl)benzoate 

Downstream Products

• 226087-15-6 2-(4-aminomethyl-benzoyl)-benzoic acid methyl ester 
• 114772-97-3 2-butyl-1-<4-(2-carbomethoxybenzoyl)benzyl>-4-chloro-5-(hydroxymethyl)imidazole 
• 114772-98-4 2-butyl-1-<4-(2-carbomethoxybenzoyl)benzyl>-4-chloro-5-(chloromethyl)imidazole hydrochloride 
• 114773-04-5 2-butyl-1-<4-(carbomethoxybenzoyl)benzyl>-4-chloro-5-<<(methoxycarbonyl)amino>methyl>imidazole 
• 114799-56-3 2-butyl-1-<4-(2-carboxybenzoyl)benzyl>-4-chloro-5-<<(methoxycarbonyl)amino>methyl>imidazole 
• 114773-01-2 5-(azidomethyl)-2-butyl-1-<4-(2-carbomethoxybenzoyl)benzyl>-4-chloroimidazole 
• 114773-03-4 2-[4-(2-Butyl-4-chloro-5-methoxymethyl-imidazol-1-ylmethyl)-benzoyl]-benzoic acid methyl ester 
• 114773-94-3 2-[4-(5-Aminomethyl-2-butyl-4-chloro-imidazol-1-ylmethyl)-benzoyl]-benzoic acid methyl ester 
• 114822-98-9 2-butyl-1-<4-(2-carboxybenzoyl)benzyl>-4-chloro-5-(methoxymethyl)imidazole 
• 114799-50-7 2-Butyl-1-[4-(2-Carboxybenzoyl)benzyl]-4-chloro-5-(hydroxymethyl)imidazole 
• 226087-17-8 2-[4-({6-[5-((3aR,6S,6aS)-2-Oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoylamino]-hexanoylamino}-methyl)-benzoyl]-benzoic acid 
• 226087-16-7 2-[4-({6-[5-((3aR,6S,6aS)-2-Oxo-hexahydro-thieno[3,4-d]imidazol-6-yl)-pentanoylamino]-hexanoylamino}-methyl)-benzoyl]-benzoic acid methyl ester 
• 291774-12-4 2-butyl-3-[4-(2-carbomethoxybenzoyl)benzyl]-2,3-diazaspiro[4.4]nonane-1,4-dione 

Relevant academic research and scientific papers

2-aroylbenzoyl serine proteases: Photoreversible inhibition or photoaffinity labeling?

Phenyl esters of 2-benzoylbenzoates were determined to be inhibitors of the serine protease enzymes chymotrypsin and thrombin. Thus, p- guanidinophenyl 2-benzoylbenzoate (lb) inhibited thrombin while the corresponding p-nitrophenyl ester (1a) inhibited ch

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