141367-76-2

Upstream product

• 39208-08-7 ethyl 3-<2-(benzyloxy)phenyl>-3-oxopropanoate 
• 62-53-3 aniline 

Downstream Products

• 141367-59-1 2-(2-Benzyloxy-phenyl)-1-phenyl-4-p-tolyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 141367-64-8 4-Benzyl-2-(2-benzyloxy-phenyl)-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 141367-40-0 3-(4-Nitro-phenyl)-1-phenyl-1H-chromeno[4,3-b]pyrrol-4-one 
• 141367-87-5 2-(2-Benzyloxy-phenyl)-4-methyl-1-phenyl-1H-pyrrole-3-carboxylic acid 
• 141367-39-7 1-Phenyl-3-p-tolyl-1H-chromeno[4,3-b]pyrrol-4-one 
• 141367-45-5 3-Benzyl-1-phenyl-1H-chromeno[4,3-b]pyrrol-4-one 
• 141368-00-5 2-(2-Hydroxy-phenyl)-4-methyl-1-phenyl-1H-pyrrole-3-carboxylic acid 
• 141367-49-9 3-Methyl-1-phenyl-1H-chromeno[4,3-b]pyrrol-4-one 
• 141367-60-4 2-(2-Benzyloxy-phenyl)-4-(4-nitro-phenyl)-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 141367-68-2 2-(2-Benzyloxy-phenyl)-4-methyl-1-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

Tricyclic heteroaromatic systems. Synthesis of 1,3 and 1,2 disubstituted [1]benzopyrano[4,3-b]pyrrol-4-ones and structure-activity relationships as benzodiazepine receptor ligands

The synthesis of some 1,3- and 1,2- disubstituted [1]benzopyrano-pyrrol-4-ones is reported as well as their benzodiazepine receptor affinity, as measured by the ability to displace [3H]flunitrazepam from its specific central binding. The struct