4-Chloro-7-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 7 positions, respectively, contributes to its unique 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 influence the compound's lipophilicity, solubility, and interaction with biological targets. Additionally, 4-chloro-7-iodoquinoline may exhibit antimicrobial or antiprotozoal 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-7-iodoquinoline with care due to potential toxicity and environmental concerns associated with halogenated organic compounds.

4-chloro-7-iodoquinoline

22200-50-6: 4-Chloro-7-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 7 positions, respectively, contributes to its unique 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 influence the compound's lipophilicity, solubility, and interaction with biological targets. Additionally, 4-chloro-7-iodoquinoline may exhibit antimicrobial or antiprotozoal 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-7-iodoquinoline with care due to potential toxicity and environmental concerns associated with halogenated organic compounds.

CAS 22200-50-6

4-chloro-7-iodoquinoline

4-Chloro-7-iodoquinoline

Ref: IN-DA006ZG2

7-Iodo-4-chloroquinoline

Ref: 10-F093012