86625-47-0

Upstream product

• 65474-26-2 ethyl 2,5-diphenyl-1H-pyrrole-3-carboxylate 

Downstream Products

• 205751-56-0 1-(2-Benzyloxy-1-benzyloxymethyl-ethoxymethyl)-4-nitro-2,5-diphenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 206350-56-3 1-(2-Acetoxyethoxy)methyl-2,5-diphenyl-3-ethoxycarbonyl-4-nitropyrrole 
• 310411-45-1 ethyl 1-methyl-4-nitro-2,5-diphenylpyrrole-3-carboxylate 
• 206350-61-0 1-(2-Acetoxyethoxy)methyl-3-amino-2,5-diphenyl-4-ethoxycarbonylpyrrole 
• 205751-64-0 1-(1,3-Dihydroxy-2-propoxy)methyl-2,5-diphenyl-3-ethoxycarbonyl-4-nitropyrrole 
• 205751-67-3 4-Amino-1-(1,3-dihydroxy-2-propoxy)methyl-3-ethoxycarbonyl-2,5-diphenylpyrrole 
• 86625-50-5 4-Amino-2,5-diphenyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 310411-57-5 7-methyl-3,6,8-triphenyl-5,7-dihydro-4H-pyrrolo[3,4-e][1,2,3]triazolo[1,5-a]pyrimidine-5-one 
• 310411-48-4 ethyl 4-amino-1-methyl-2,5-diphenylpyrrole-3-carboxylate 
• 310411-51-9 ethyl 4-azido-1-methyl-2,5-diphenyl-1H-pyrrole-3-carboxylate 

Relevant academic research and scientific papers

3-Diazopyrroles. Part 5 (1). Antibacterial activity of 3-diazo-2-phenylpyrroles

3-Diazo-2-phenylpyrroles 3a-g showed antimicrobial activity against Gram-positive bacteria, whereas against Gram-negative strains the inhibitory activity is limited to derivatives 3a and 3c. The substituents at 4 and 5 positions strongly influence the inh

REACTIVITY OF 3-DIAZOPYRROLES. PART 2.

3-Diazopyrroles 8 were prepared as key compounds for an alternative route to synthetize 1H-pyrrolocinnoline. However under the acidic conditions, decomposition and intermolecular coupling reactions were only observed.