2-Chloro-6-fluoro-quinoline-3-carbonitrile is a heterocyclic organic compound characterized by a quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of a chloro group at the 2-position and a fluoro group at the 6-position introduces halogen substituents that can influence the compound's reactivity and biological activity. The carbonitrile functional group at the 3-position contributes to its polar character and can participate in various chemical reactions, such as nucleophilic additions. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its unique structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as quinoline derivatives are known for their diverse biological activities, including antimicrobial and antimalarial properties. Additionally, the specific arrangement of substituents can affect the compound's electronic properties, making it a subject of interest in material science and organic synthesis. Safety data should be consulted for handling and usage, as halogenated compounds can pose health risks.

2-chloro-6-fluoro-quinoline-3-carbonitrile

948291-71-2: 2-Chloro-6-fluoro-quinoline-3-carbonitrile is a heterocyclic organic compound characterized by a quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of a chloro group at the 2-position and a fluoro group at the 6-position introduces halogen substituents that can influence the compound's reactivity and biological activity. The carbonitrile functional group at the 3-position contributes to its polar character and can participate in various chemical reactions, such as nucleophilic additions. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its unique structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as quinoline derivatives are known for their diverse biological activities, including antimicrobial and antimalarial properties. Additionally, the specific arrangement of substituents can affect the compound's electronic properties, making it a subject of interest in material science and organic synthesis. Safety data should be consulted for handling and usage, as halogenated compounds can pose health risks.

2-Chloro-6-fluoroquinoline-3-carbonitrile

CAS 948291-71-2

2-chloro-6-fluoro-quinoline-3-carbonitrile

2-Chloro-6-fluoroquinoline-3-carbonitrile

Ref: 54-PC404557