4,7-Dimethyl-1H-indole-2-carboxylic acid is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features two methyl groups at the 4 and 7 positions of the indole ring and a carboxylic acid functional group at the 2 position. The presence of these functional groups contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and organic synthesis. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid group. Its molecular structure allows for potential interactions with biological systems, making it of interest in medicinal chemistry. Additionally, the compound may undergo typical reactions associated with carboxylic acids, such as esterification and decarboxylation, and can participate in electrophilic aromatic substitution due to the electron-donating nature of the methyl groups. Overall, 4,7-dimethyl-1H-indole-2-carboxylic acid is a versatile compound with significant implications in chemical research and development.

4,7-DIMETHYL-1H-INDOLE-2-CARBOXYLIC ACID

103988-96-1: 4,7-Dimethyl-1H-indole-2-carboxylic acid is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features two methyl groups at the 4 and 7 positions of the indole ring and a carboxylic acid functional group at the 2 position. The presence of these functional groups contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and organic synthesis. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid group. Its molecular structure allows for potential interactions with biological systems, making it of interest in medicinal chemistry. Additionally, the compound may undergo typical reactions associated with carboxylic acids, such as esterification and decarboxylation, and can participate in electrophilic aromatic substitution due to the electron-donating nature of the methyl groups. Overall, 4,7-dimethyl-1H-indole-2-carboxylic acid is a versatile compound with significant implications in chemical research and development.

CAS 103988-96-1

4,7-DIMETHYL-1H-INDOLE-2-CARBOXYLIC ACID

4,7-Dimethyl-1H-indole-2-carboxylic acid

Ref: 54-OR904418

4,7-Dimethyl-1H-indole-2-carboxylic acid

Ref: 3D-DEA98896