4-Chloro-7-fluoroquinoline is a heterocyclic compound belonging to the quinoline family, characterized by a bicyclic structure that includes a benzene ring fused to a pyridine ring. This compound features a chlorine atom at the 4-position and a fluorine atom at the 7-position of the quinoline ring, which can influence its chemical reactivity and biological activity. It is typically a pale yellow to light brown solid, with moderate solubility in organic solvents. The presence of halogen substituents often enhances the compound's pharmacological properties, making it of interest in medicinal chemistry, particularly in the development of antimicrobial and antiviral agents. Additionally, 4-chloro-7-fluoroquinoline may exhibit unique electronic properties due to the electronegative halogens, which can affect its interaction with biological targets. Safety data indicates that, like many halogenated compounds, it should be handled with care to avoid potential health hazards. Overall, its structural characteristics and substituents contribute to its potential applications in various fields, including pharmaceuticals and agrochemicals.

4-chloro-7-fluoroquinoline

391-82-2: 4-Chloro-7-fluoroquinoline is a heterocyclic compound belonging to the quinoline family, characterized by a bicyclic structure that includes a benzene ring fused to a pyridine ring. This compound features a chlorine atom at the 4-position and a fluorine atom at the 7-position of the quinoline ring, which can influence its chemical reactivity and biological activity. It is typically a pale yellow to light brown solid, with moderate solubility in organic solvents. The presence of halogen substituents often enhances the compound's pharmacological properties, making it of interest in medicinal chemistry, particularly in the development of antimicrobial and antiviral agents. Additionally, 4-chloro-7-fluoroquinoline may exhibit unique electronic properties due to the electronegative halogens, which can affect its interaction with biological targets. Safety data indicates that, like many halogenated compounds, it should be handled with care to avoid potential health hazards. Overall, its structural characteristics and substituents contribute to its potential applications in various fields, including pharmaceuticals and agrochemicals.

CAS 391-82-2

4-chloro-7-fluoroquinoline

4-Chloro-7-fluoroquinoline

Ref: IN-DA0037I9

4-Chloro-7-fluoroquinoline

Ref: 54-PC404563

4-Chloro-7-fluoroquinoline

Ref: 10-F225930