6-Chloro-5-iodo-1H-indole is a heterocyclic organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of chlorine and iodine substituents at the 6 and 5 positions, respectively, significantly influences its chemical reactivity and properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific solvent used. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with indole derivatives. The halogen substituents can enhance the compound's lipophilicity and influence its interaction with biological targets. Additionally, 6-Chloro-5-iodo-1H-indole may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in organic synthesis. Safety data should be consulted for handling, as halogenated compounds can pose health risks.

6-Chloro-5-iodo-1H-indole

122509-74-4: 6-Chloro-5-iodo-1H-indole is a heterocyclic organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of chlorine and iodine substituents at the 6 and 5 positions, respectively, significantly influences its chemical reactivity and properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents, depending on the specific solvent used. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with indole derivatives. The halogen substituents can enhance the compound's lipophilicity and influence its interaction with biological targets. Additionally, 6-Chloro-5-iodo-1H-indole may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in organic synthesis. Safety data should be consulted for handling, as halogenated compounds can pose health risks.

CAS 122509-74-4

6-Chloro-5-iodo-1H-indole

6-chloro-5-iodo-1H-indole

Ref: IN-DA0017CN