Quinoline, 2-chloro-6-fluoro- is an aromatic heterocyclic compound characterized by a quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of a chlorine atom at the second position and a fluorine atom at the sixth position of the quinoline structure imparts unique chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is known for its potential applications in pharmaceuticals, agrochemicals, and as an intermediate in organic synthesis. The presence of halogen substituents can influence its reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, quinoline derivatives are often studied for their biological activities, including antimicrobial and antimalarial properties. Safety data should be consulted, as halogenated compounds can exhibit toxicity and environmental persistence. Overall, 2-chloro-6-fluoro-quinoline represents a significant compound in both industrial and research contexts.

Quinoline,2-chloro-6-fluoro-

77119-53-0: Quinoline, 2-chloro-6-fluoro- is an aromatic heterocyclic compound characterized by a quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of a chlorine atom at the second position and a fluorine atom at the sixth position of the quinoline structure imparts unique chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is known for its potential applications in pharmaceuticals, agrochemicals, and as an intermediate in organic synthesis. The presence of halogen substituents can influence its reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, quinoline derivatives are often studied for their biological activities, including antimicrobial and antimalarial properties. Safety data should be consulted, as halogenated compounds can exhibit toxicity and environmental persistence. Overall, 2-chloro-6-fluoro-quinoline represents a significant compound in both industrial and research contexts.

CAS 77119-53-0

Quinoline,2-chloro-6-fluoro-

2-Chloro-6-fluoroquinoline

Ref: IN-DA008NZP

2-Chloro-6-fluoroquinoline

Ref: 54-PC404621

2-Chloro-6-fluoroquinoline

Ref: 10-F215816