4-Chloro-6-iodoquinoline is a heterocyclic organic compound characterized by a quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of chlorine and iodine substituents at the 4 and 6 positions, respectively, significantly influences its chemical properties and reactivity. This compound typically appears as a solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The halogen substituents can enhance the compound's lipophilicity and influence its interaction with biological targets. Additionally, 4-Chloro-6-iodoquinoline may exhibit antimicrobial or antitumor properties, making it of interest in drug discovery. Its synthesis often involves halogenation reactions and can be achieved through various methods, including electrophilic aromatic substitution. As with many halogenated compounds, it is essential to handle 4-Chloro-6-iodoquinoline with care due to potential toxicity and environmental concerns associated with halogenated organic compounds.

4-Chloro-6-iodoquinoline

4-Chloro-6-iodoquinoline is a quinoline derivative that has been used as a building block in organic synthesis. It is typically prepared by the reaction of an acid chloride with chlorine or by chlorination of an aromatic ring. The compound has been used in cross-coupling reactions, halogenation, and crystallography. 4-Chloro-6-iodoquinoline can be prepared from dimethylacetylenedicarboxylate and chlorides or halides. This product can also be synthesized using the Suzuki reaction.

CAS 40107-07-1: 4-Chloro-6-iodoquinoline

4-Chloro-6-iodoquinoline

Ref: 54-OR94279

4-Chloro-6-iodoquinoline

Ref: 10-F227886

4-Chloro-6-iodoquinoline

Ref: 3D-FC57757

4-CHLORO-6-IODOQUINOLINE

Ref: IN-DA00BYHZ