4-Methyl-1H-indole-6-carboxylic acid is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a carboxylic acid functional group (-COOH) at the 6-position and a methyl group (-CH3) at the 4-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is soluble in polar solvents due to the carboxylic acid group, which can engage in hydrogen bonding. It may exhibit acidic behavior, capable of donating a proton in solution. The indole moiety is known for its biological significance, often found in various natural products and pharmaceuticals, suggesting potential applications in medicinal chemistry. Additionally, the compound may participate in various chemical reactions, including esterification and amidation, due to the reactive carboxylic acid group. Its specific reactivity and interactions can be influenced by the presence of the methyl group, which can affect steric hindrance and electronic properties. Overall, 4-methyl-1H-indole-6-carboxylic acid is a compound of interest in both synthetic and medicinal chemistry contexts.

4-methyl-1H-indole-6-carboxylic acid

1545472-15-8: 4-Methyl-1H-indole-6-carboxylic acid is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a carboxylic acid functional group (-COOH) at the 6-position and a methyl group (-CH3) at the 4-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is soluble in polar solvents due to the carboxylic acid group, which can engage in hydrogen bonding. It may exhibit acidic behavior, capable of donating a proton in solution. The indole moiety is known for its biological significance, often found in various natural products and pharmaceuticals, suggesting potential applications in medicinal chemistry. Additionally, the compound may participate in various chemical reactions, including esterification and amidation, due to the reactive carboxylic acid group. Its specific reactivity and interactions can be influenced by the presence of the methyl group, which can affect steric hindrance and electronic properties. Overall, 4-methyl-1H-indole-6-carboxylic acid is a compound of interest in both synthetic and medicinal chemistry contexts.

CAS 1545472-15-8

4-methyl-1H-indole-6-carboxylic acid

4-Methyl-1H-indole-6-carboxylic acid

Ref: 54-OR1057605

4-Methyl-1H-indole-6-carboxylic acid

Ref: 10-F540251