4-Chloro-8-cyanoquinoline 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 4-position and a cyano group at the 8-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. It is known for its potential applications in pharmaceuticals, particularly as a building block in the synthesis of various bioactive molecules. The cyano group can participate in nucleophilic reactions, while the chloro group can serve as a leaving group in substitution reactions. Additionally, 4-chloro-8-cyanoquinoline may exhibit interesting photophysical properties, making it a candidate for studies in materials science and organic electronics. As with many quinoline derivatives, it may also possess biological activity, warranting further investigation into its pharmacological potential. Safety data should be consulted, as halogenated compounds can pose environmental and health risks.

4-CHLORO-8-CYANOQUINOLINE

132664-45-0: 4-Chloro-8-cyanoquinoline 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 4-position and a cyano group at the 8-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. It is known for its potential applications in pharmaceuticals, particularly as a building block in the synthesis of various bioactive molecules. The cyano group can participate in nucleophilic reactions, while the chloro group can serve as a leaving group in substitution reactions. Additionally, 4-chloro-8-cyanoquinoline may exhibit interesting photophysical properties, making it a candidate for studies in materials science and organic electronics. As with many quinoline derivatives, it may also possess biological activity, warranting further investigation into its pharmacological potential. Safety data should be consulted, as halogenated compounds can pose environmental and health risks.

CAS 132664-45-0

4-CHLORO-8-CYANOQUINOLINE

8-Quinolinecarbonitrile, 4-chloro-

Ref: IN-DA0010XX

4-Chloroquinoline-8-carbonitrile

Ref: 54-OR87424

4-Chloroquinoline-8-carbonitrile

Ref: 10-F619437