4424-76-4

Usage

Class of chemical

Pyrrole

Uses

Building block for synthesizing various drugs and pesticides in pharmaceutical and agrochemical industries, solvent in industrial processes, flavor and fragrance ingredient in cosmetics and personal care products industry

Physical form

White to off-white crystalline powder

Molecular weight

243.3 g/mol

Biological activities

Potential for various biological activities, with derivatives exhibiting anticancer, anticonvulsant, and antimicrobial properties.

Upstream product

• 5396-89-4 benzyl acetoacetate 
• 2199-46-4 2-(ethoxycarbonyl)-3,4,5-trimethylpyrrole 
• 100-51-6 benzyl alcohol 
• 69912-09-0 3,5-dimethylpyrrole-2,4-dicarboxylic acid 2-benzyl ester 
• 69912-08-9 benzyl 4-t-butoxycarbonyl-3,5-dimethylpyrrole-2-carboxylate 

Downstream Products

• 65038-94-0 5-((acetoxy)methyl)-2-((benzyloxy)carbonyl)-3,4-dimethylpyrrole 
• 17106-08-0 3,4,5-trimethyl-2-pyrrolecarboxylic acid 
• 92578-75-1 5-bromomethyl-3,4-dimethyl-pyrrole-2-carboxylic acid benzyl ester 
• 59435-08-4 benzyl 5-formyl-3,4-dimethylpyrrole-2-carboxylate 
• 86568-85-6 2-((benzyloxy)carbonyl)-5-((tert-butyloxy)carbonyl)-3,4-dimethylpyrrole 
• 27226-50-2 3,4,5-trimethyl-1H-pyrrole-2-carbaldehyde 
• 124281-51-2 3,13-diethyl-1,2,7,8,12,17,18,19-octamethyl-10,23-dihydrobilin dihydrobromide 
• 124281-50-1 2,13-diethyl-1,3,7,8,12,17,18,19-octamethyl-10,23-dihydrobilin dihydrobromide 
• 738550-33-9 benzyl 8-ethyl-2,7,12,13,14-pentamethyl-5,16-dihydrotripyrrin-1-carboxylate 
• 739335-33-2 benzyl 8-ethyl-2,3,7,12,13,14-hexamethyl-5,16-dihydrotripyrrin-1-carboxylate 
• 783269-49-8 benzyl 3,8-diethyl-2,7,12,13,14-pentamethyl-5,16-dihydrotripyrrin-1-carboxylate 
• 86568-89-0 5-((benzyloxy)carbonyl)-3,3',4,4'-tetramethyl-2,2'-dipyrromethane 
• 86568-88-9 5-[(benzyloxy)carbonyl]-5'-[(tert-butyloxy)carbonyl]-3,3',4,4'-tetramethyl-2,2'-dipyrromethane 
• 86568-90-3 5-((benzyloxy)carbonyl)-3,3',4,4'-tetramethyl-5'-(5-((benzyloxy)carbonyl)-3,4-dimethylpyrrol-2-yl)-2,2'-dipyrromethene hydrochloride 

Relevant academic research and scientific papers

TOTAL SYNTHESES OF MONO-, DI-, AND TRI-PROPIONIC PORPHYRINS FOR STUDIES OF THE MECHANISM OF HEME-APOPROTEIN RECONSTITUTION

Total syntheses of eight new porphyrins bearing either one (14), two (8, 15, 28, 29, 51) or three (42, 43) propionic side chains in variously permutated positions around the porphyrin periphery are described.Compound (8) was prepared using the MacDonald (

Sapphyrins: Novel Aromatic Pentapyrrolic Macrocycles

Sapphyrins are pentapyrrolic macrocycles containing one direct link and four bridging methine groups between the five pyrrolic subunits.The syntheses of decamethylsapphyrin, other peripherally alkylated derivatives, and metal complexes are described.The p