5-Chloro-2-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 5 and 2 positions, respectively, introduces significant reactivity and influences its chemical properties. This compound typically exhibits a pale yellow to brownish appearance and is soluble in organic solvents. Its molecular structure allows for 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 may affect its interaction with biological targets. Additionally, 5-Chloro-2-iodo-1H-indole may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a valuable intermediate in organic synthesis. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, this compound is of interest in both research and industrial applications due to its unique structural features and reactivity.

5-Chloro-2-iodo-1H-indole

1388032-50-5: 5-Chloro-2-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 5 and 2 positions, respectively, introduces significant reactivity and influences its chemical properties. This compound typically exhibits a pale yellow to brownish appearance and is soluble in organic solvents. Its molecular structure allows for 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 may affect its interaction with biological targets. Additionally, 5-Chloro-2-iodo-1H-indole may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a valuable intermediate in organic synthesis. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, this compound is of interest in both research and industrial applications due to its unique structural features and reactivity.

CAS 1388032-50-5

5-Chloro-2-iodo-1H-indole

5-Chloro-2-iodo-1H-indole

Ref: IN-DA00HVBS

5-Chloro-2-iodoindole

Ref: 54-OR471570

5-CHLORO-2-IODO-1H-INDOLE

Ref: 10-F530092