5,6-Dichloro-1H-indole-3-carbaldehyde 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 chlorine atoms at the 5 and 6 positions of the indole ring contributes to its reactivity and potential biological activity. The aldehyde functional group at the 3-position makes it a versatile intermediate in organic synthesis, allowing for further chemical modifications. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its unique structure suggests potential applications in pharmaceuticals, agrochemicals, and materials science. Additionally, the dichloro substitution can enhance its properties, such as increased lipophilicity or altered electronic characteristics, which may influence its interaction with biological targets. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 5,6-dichloro-1H-indole-3-carbaldehyde is a significant compound in synthetic organic chemistry with potential applications in various fields.

5,6-dichloro-1H-indole-3-carbaldehyde

1227578-94-0: 5,6-Dichloro-1H-indole-3-carbaldehyde 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 chlorine atoms at the 5 and 6 positions of the indole ring contributes to its reactivity and potential biological activity. The aldehyde functional group at the 3-position makes it a versatile intermediate in organic synthesis, allowing for further chemical modifications. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its unique structure suggests potential applications in pharmaceuticals, agrochemicals, and materials science. Additionally, the dichloro substitution can enhance its properties, such as increased lipophilicity or altered electronic characteristics, which may influence its interaction with biological targets. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 5,6-dichloro-1H-indole-3-carbaldehyde is a significant compound in synthetic organic chemistry with potential applications in various fields.

CAS 1227578-94-0

5,6-dichloro-1H-indole-3-carbaldehyde

1H-Indole-3-carboxaldehyde, 5,6-dichloro-

Ref: IN-DA000JBR

5,6-Dichloro-1H-indole-3-carbaldehyde

Ref: 10-F455464