4-(4-Methylphenyl)-1H-pyrrole-3-carboxylic acid methyl ester, identified by CAS number 188524-66-5, is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. This compound features a methyl ester functional group, contributing to its solubility in organic solvents and potential reactivity in various chemical reactions. The presence of the 4-methylphenyl group enhances its hydrophobic characteristics and may influence its biological activity. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The molecular structure suggests that it may exhibit interesting electronic properties due to the conjugation between the aromatic and heterocyclic systems. Additionally, the carboxylic acid moiety, even in its esterified form, can participate in hydrogen bonding, which may affect its interactions with biological targets or other chemical species. Overall, this compound's unique structure and functional groups make it a subject of interest in various fields of chemical research.

4-(4-METHYLPHENYL)-1H-PYRROLE-3-CARBOXYLICACIDMETHYLESTER

188524-66-5: 4-(4-Methylphenyl)-1H-pyrrole-3-carboxylic acid methyl ester, identified by CAS number 188524-66-5, is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. This compound features a methyl ester functional group, contributing to its solubility in organic solvents and potential reactivity in various chemical reactions. The presence of the 4-methylphenyl group enhances its hydrophobic characteristics and may influence its biological activity. Typically, compounds of this nature are studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. The molecular structure suggests that it may exhibit interesting electronic properties due to the conjugation between the aromatic and heterocyclic systems. Additionally, the carboxylic acid moiety, even in its esterified form, can participate in hydrogen bonding, which may affect its interactions with biological targets or other chemical species. Overall, this compound's unique structure and functional groups make it a subject of interest in various fields of chemical research.

1H-Pyrrole-3-carboxylic acid, 4-(4-methylphenyl)-, methyl ester

<p>4-p-Tolyl-1H-pyrrole-3-carboxylic acid methyl ester</p>

CAS 188524-66-5

4-(4-METHYLPHENYL)-1H-PYRROLE-3-CARBOXYLICACIDMETHYLESTER

1H-Pyrrole-3-carboxylic acid, 4-(4-methylphenyl)-, methyl ester

Ref: IN-DA002GYD

4-p-Tolyl-1H-pyrrole-3-carboxylic acid methyl ester

Ref: 54-OR346619

4-p-Tolyl-1H-pyrrole-3-carboxylic acid methyl ester

Ref: 10-F521915