4-(4-Methylphenyl)-1H-pyrrole-3-carboxylic acid, with the CAS number 191668-22-1, is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. This compound features a carboxylic acid functional group (-COOH) at the 3-position of the pyrrole ring, contributing to its acidic properties. The presence of a 4-methylphenyl group at the 4-position enhances its hydrophobic characteristics and may influence its solubility and reactivity. Typically, compounds like this can exhibit biological activity, making them of interest in pharmaceutical research. The molecular structure suggests potential for hydrogen bonding due to the carboxylic acid, which can affect its interactions in biological systems. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the methyl and phenyl substituents. Overall, this compound's unique structure and functional groups make it a subject of interest in various chemical and biological applications.

4-(4-METHYLPHENYL)-1H-PYRROLE-3-CARBOXYLIC ACID

191668-22-1: 4-(4-Methylphenyl)-1H-pyrrole-3-carboxylic acid, with the CAS number 191668-22-1, is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. This compound features a carboxylic acid functional group (-COOH) at the 3-position of the pyrrole ring, contributing to its acidic properties. The presence of a 4-methylphenyl group at the 4-position enhances its hydrophobic characteristics and may influence its solubility and reactivity. Typically, compounds like this can exhibit biological activity, making them of interest in pharmaceutical research. The molecular structure suggests potential for hydrogen bonding due to the carboxylic acid, which can affect its interactions in biological systems. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the methyl and phenyl substituents. Overall, this compound's unique structure and functional groups make it a subject of interest in various chemical and biological applications.

CAS 191668-22-1

4-(4-METHYLPHENYL)-1H-PYRROLE-3-CARBOXYLIC ACID

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

Ref: IN-DA002FF2

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

Ref: 54-OR346621

4-(P-tolyl)-1H-pyrrole-3-carboxylic acid

Ref: 10-F725178