Methyl 3-methyl-1H-indole-5-carboxylate, with the CAS number 588688-33-9, is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a methyl group at the 3-position and a carboxylate ester functional group at the 5-position, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the methyl group enhances its lipophilicity, which may influence its biological activity and solubility in organic solvents. Methyl 3-methyl-1H-indole-5-carboxylate may be utilized in various chemical reactions, including as an intermediate in the synthesis of pharmaceuticals or agrochemicals. Its specific properties, such as boiling point, melting point, and spectral characteristics, can vary based on the conditions and methods of synthesis. As with many indole derivatives, it may exhibit interesting biological activities, warranting further investigation in medicinal chemistry.

methyl 3-methyl-1H-indole-5-carboxylate

588688-33-9: Methyl 3-methyl-1H-indole-5-carboxylate, with the CAS number 588688-33-9, is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a methyl group at the 3-position and a carboxylate ester functional group at the 5-position, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the methyl group enhances its lipophilicity, which may influence its biological activity and solubility in organic solvents. Methyl 3-methyl-1H-indole-5-carboxylate may be utilized in various chemical reactions, including as an intermediate in the synthesis of pharmaceuticals or agrochemicals. Its specific properties, such as boiling point, melting point, and spectral characteristics, can vary based on the conditions and methods of synthesis. As with many indole derivatives, it may exhibit interesting biological activities, warranting further investigation in medicinal chemistry.

CAS 588688-33-9

methyl 3-methyl-1H-indole-5-carboxylate

Methyl 3-methyl-1H-indole-5-carboxylate

Ref: IN-DA00ELNM

Methyl 3-methyl-1H-indole-5-carboxylate

Ref: 54-OR62081

Methyl 3-methyl-1H-indole-5-carboxylate

Ref: 10-F234453