2-Chloro-1-methyl-1H-indole-3,5-dicarbaldehyde is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of two aldehyde groups at the 3 and 5 positions of the indole ring contributes to its reactivity, making it a valuable intermediate in organic synthesis. The chlorine substituent at the 2-position enhances its electrophilic properties, allowing for further chemical modifications. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its unique structure allows it to participate in various chemical reactions, including condensation and substitution reactions, which are useful in the synthesis of more complex molecules. Additionally, due to the presence of functional groups, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks similar to other chlorinated organic compounds.

2-chloro-1-methyl-1H-indole-3,5-dicarbaldehyde

66335-32-8: 2-Chloro-1-methyl-1H-indole-3,5-dicarbaldehyde is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of two aldehyde groups at the 3 and 5 positions of the indole ring contributes to its reactivity, making it a valuable intermediate in organic synthesis. The chlorine substituent at the 2-position enhances its electrophilic properties, allowing for further chemical modifications. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its unique structure allows it to participate in various chemical reactions, including condensation and substitution reactions, which are useful in the synthesis of more complex molecules. Additionally, due to the presence of functional groups, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks similar to other chlorinated organic compounds.

CAS 66335-32-8

2-chloro-1-methyl-1H-indole-3,5-dicarbaldehyde

2-Chloro-1-methyl-1H-indole-3,5-dicarbaldehyde

Ref: 3D-RCA33532