1H-Indole-3-carboxylic acid, 7-methyl-, methyl ester, identified by CAS number 773134-49-9, is an organic compound belonging to the indole family, characterized by its bicyclic structure that includes a fused benzene and pyrrole ring. This compound features a carboxylic acid functional group and a methyl ester, which contribute to its chemical reactivity and solubility properties. Typically, indole derivatives exhibit biological activity, making them of interest in pharmaceutical research. The presence of the methyl group at the 7-position of the indole ring can influence the compound's electronic properties and steric hindrance, potentially affecting its interaction with biological targets. In terms of physical properties, such compounds are often crystalline solids at room temperature and may exhibit moderate to high solubility in organic solvents. The compound's reactivity can be attributed to the functional groups present, allowing for various chemical transformations, including esterification and substitution reactions. Overall, 1H-indole-3-carboxylic acid, 7-methyl-, methyl ester is a significant compound in organic synthesis and medicinal chemistry.

1H-indole-3-carboxylic acid, 7-methyl-, methyl ester

773134-49-9: 1H-Indole-3-carboxylic acid, 7-methyl-, methyl ester, identified by CAS number 773134-49-9, is an organic compound belonging to the indole family, characterized by its bicyclic structure that includes a fused benzene and pyrrole ring. This compound features a carboxylic acid functional group and a methyl ester, which contribute to its chemical reactivity and solubility properties. Typically, indole derivatives exhibit biological activity, making them of interest in pharmaceutical research. The presence of the methyl group at the 7-position of the indole ring can influence the compound's electronic properties and steric hindrance, potentially affecting its interaction with biological targets. In terms of physical properties, such compounds are often crystalline solids at room temperature and may exhibit moderate to high solubility in organic solvents. The compound's reactivity can be attributed to the functional groups present, allowing for various chemical transformations, including esterification and substitution reactions. Overall, 1H-indole-3-carboxylic acid, 7-methyl-, methyl ester is a significant compound in organic synthesis and medicinal chemistry.

CAS 773134-49-9

1H-indole-3-carboxylic acid, 7-methyl-, methyl ester

METHYL 7-METHYL-1H-INDOLE-3-CARBOXYLATE

Ref: IN-DA005NPW

Methyl 7-methyl-1H-indole-3-carboxylate

Ref: 54-OR90414

Methyl 7-methyl-1H-indole-3-carboxylate

Ref: 10-F093455