Quinoline, 3-fluoro-4-iodo- is an organic compound characterized by its heterocyclic structure, which includes a fused benzene and pyridine ring. The presence of a fluorine atom at the 3-position and an iodine atom at the 4-position of the quinoline ring significantly influences its chemical properties and reactivity. This compound is typically a pale yellow to brown solid and is soluble in organic solvents. It exhibits interesting biological activities, making it a subject of research in medicinal chemistry. The presence of halogen substituents can enhance its potential as a building block in the synthesis of pharmaceuticals and agrochemicals. Additionally, the compound may participate in various chemical reactions, such as nucleophilic substitutions and electrophilic aromatic substitutions, due to the electron-withdrawing nature of the halogens. Its unique structure and substituents contribute to its potential applications in various fields, including materials science and organic synthesis. Safety data should be consulted for handling and storage, as halogenated compounds can pose specific health and environmental risks.

Quinoline,3-fluoro-4-iodo-

213772-63-5: Quinoline, 3-fluoro-4-iodo- is an organic compound characterized by its heterocyclic structure, which includes a fused benzene and pyridine ring. The presence of a fluorine atom at the 3-position and an iodine atom at the 4-position of the quinoline ring significantly influences its chemical properties and reactivity. This compound is typically a pale yellow to brown solid and is soluble in organic solvents. It exhibits interesting biological activities, making it a subject of research in medicinal chemistry. The presence of halogen substituents can enhance its potential as a building block in the synthesis of pharmaceuticals and agrochemicals. Additionally, the compound may participate in various chemical reactions, such as nucleophilic substitutions and electrophilic aromatic substitutions, due to the electron-withdrawing nature of the halogens. Its unique structure and substituents contribute to its potential applications in various fields, including materials science and organic synthesis. Safety data should be consulted for handling and storage, as halogenated compounds can pose specific health and environmental risks.

CAS 213772-63-5

Quinoline,3-fluoro-4-iodo-

Quinoline,3-fluoro-4-iodo-

Ref: IN-DA007QNU

3-Fluoro-4-iodoquinoline

Ref: 10-F733086