6-Iodoquinolin-4(1H)-one is a chemical compound characterized by its quinoline structure, which features a nitrogen atom within a bicyclic aromatic system. The presence of an iodine atom at the 6-position and a carbonyl group at the 4-position contributes to its unique reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the quinoline moiety, which is known for various biological activities, including antimicrobial and anticancer properties. The iodine substituent can also enhance the compound's lipophilicity and influence its interaction with biological targets. Additionally, 6-iodoquinolin-4(1H)-one may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a valuable intermediate in organic synthesis. As with many halogenated compounds, safety precautions should be observed when handling this substance due to potential toxicity and environmental concerns.

6-iodoquinolin-4(1H)-one

342617-07-6: 6-Iodoquinolin-4(1H)-one is a chemical compound characterized by its quinoline structure, which features a nitrogen atom within a bicyclic aromatic system. The presence of an iodine atom at the 6-position and a carbonyl group at the 4-position contributes to its unique reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the quinoline moiety, which is known for various biological activities, including antimicrobial and anticancer properties. The iodine substituent can also enhance the compound's lipophilicity and influence its interaction with biological targets. Additionally, 6-iodoquinolin-4(1H)-one may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a valuable intermediate in organic synthesis. As with many halogenated compounds, safety precautions should be observed when handling this substance due to potential toxicity and environmental concerns.

CAS 342617-07-6

6-iodoquinolin-4(1H)-one

4-Hydroxy-6-iodoquinoline

Ref: IN-DA007H0P

6-Iodo-1,4-dihydroquinolin-4-one

Ref: 54-OR1005800

4-Hydroxy-6-iodoquinoline

Ref: 10-F093285