5-Chloro-1-benzothiophene-3-carbaldehyde is an organic compound characterized by its unique structure, which includes a benzothiophene ring system substituted with a chlorine atom and an aldehyde functional group. The presence of the chlorine atom contributes to its reactivity and potential applications in various chemical reactions, such as electrophilic substitution. The aldehyde group is known for its reactivity in condensation reactions and can serve as a precursor for synthesizing more complex molecules. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its chemical properties make it of interest in fields such as medicinal chemistry and materials science, where it may be utilized in the synthesis of pharmaceuticals or as a building block in organic synthesis. Additionally, the compound's structure suggests potential applications in the development of dyes or agrochemicals. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

5-chloro-1-benzothiophene-3-carbaldehyde

16296-68-7: 5-Chloro-1-benzothiophene-3-carbaldehyde is an organic compound characterized by its unique structure, which includes a benzothiophene ring system substituted with a chlorine atom and an aldehyde functional group. The presence of the chlorine atom contributes to its reactivity and potential applications in various chemical reactions, such as electrophilic substitution. The aldehyde group is known for its reactivity in condensation reactions and can serve as a precursor for synthesizing more complex molecules. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its chemical properties make it of interest in fields such as medicinal chemistry and materials science, where it may be utilized in the synthesis of pharmaceuticals or as a building block in organic synthesis. Additionally, the compound's structure suggests potential applications in the development of dyes or agrochemicals. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

CAS 16296-68-7

5-chloro-1-benzothiophene-3-carbaldehyde

Benzo[b]thiophene-3-carboxaldehyde, 5-chloro-

Ref: IN-DA001TKU

5-Chlorobenzo[b]thiophene-3-carboxaldehyde

Ref: 54-OR29527

5-Chlorobenzo[b]thiophene-3-carbaldehyde

Ref: 10-F437392

5-chlorobenzo[b]thiophene-3-carbaldehyde

Ref: 3D-RAA29668