124901-13-9

Basic information

• Product Name: ethyl 4-methyl-3-(p-tolyl)-2-pyrrolecarboxylate
• Synonyms: ethyl 4-methyl-3-(p-tolyl)-2-pyrrolecarboxylate
• CAS NO: 124901-13-9
• Molecular Weight: 243.305
• Mol File: 124901-13-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 4-methyl-3-(p-tolyl)-2-pyrrolecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 4-methyl-3-(p-tolyl)-2-pyrrolecarboxylate(124901-13-9)
• EPA Substance Registry System: ethyl 4-methyl-3-(p-tolyl)-2-pyrrolecarboxylate(124901-13-9)

Safety Data

• Hazardous Substances Data: 124901-13-9(Hazardous Substances Data)

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 2999-46-4 Ethyl isocyanoacetate 
• 52287-56-6 1-(p-tolyl)-2-nitropropene 

Downstream Products

• 959849-33-3 4-methyl-1-(4-methylbenzyl)-3-p-tolyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 145101-15-1 (1-Methanesulfonyl-4-methyl-3-p-tolyl-1H-pyrrol-2-yl)-methanol 
• 124901-17-3 2,7,12,17-tetramethyl-3,8,13,18-tetra(p-tolyl)porphyrin 
• 184422-59-1 4-Methyl-5-(toluene-4-sulfonyl)-3-p-tolyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 184422-65-9 4-Methyl-5-(toluene-4-sulfonyl)-3-p-tolyl-1H-pyrrole-2-carboxylic acid 
• 184422-72-8 2-Iodo-4-methyl-5-(toluene-4-sulfonyl)-3-p-tolyl-1H-pyrrole 
• 184422-54-6 5-Iodo-4-methyl-3-p-tolyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 145101-11-7 ethyl 4-methyl-1-methylsulfonyl-3-(p-tolyl)-2-pyrrolecarboxylate 
• 145101-35-5 (4-Methyl-3-p-tolyl-1H-pyrrol-2-yl)-methanol 

Relevant articles and documents

1,3-Disubstituted 4-methyl-1H-pyrrole-2-carboxamides and their Use in Medicaments

1,3-disubstituted 4-methyl-1H-pyrrole-2-carboxamides corresponding to formula I methods for their production, pharmaceutical compositions containing them, and the use thereof for noradrenalin receptor regulation, particularly for inhibiting noradrenalin reuptake, and/or for 5-HT receptor regulation, particularly for inhibiting 5-hydroxy tryptophan reuptake, and/or for opioid receptor regulation and/or for batrachotoxin (BTX) receptor regulation and/or for treating or inhibiting pain and other conditions.

Synthesis of 2,7,12,17-Tetra-arylporphyrins, New Sterically Hindered Porphyrins

Sterically hindered porphyrins with four bulky aryl groups in the β-positions are prepared by the reduction of ethyl 3-aryl-4-alkylpyrrole-2-carboxylate with LiAlH4 followed by treatment with an acid and oxidizing agent.