4-Chloro-6,8-dimethyl-2-phenyl-quinoline is a synthetic organic compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. This compound features a chlorine atom at the 4-position and two methyl groups at the 6 and 8 positions, along with a phenyl group at the 2-position, contributing to its unique chemical properties. The presence of these substituents can influence its reactivity, solubility, and potential biological activity. Typically, quinoline derivatives are known for their applications in pharmaceuticals, agrochemicals, and as dyes. The chlorine and methyl groups can enhance lipophilicity, potentially affecting the compound's interaction with biological systems. Additionally, the compound may exhibit fluorescence, making it useful in various analytical applications. As with many organic compounds, its stability, reactivity, and potential toxicity would depend on environmental conditions and specific functional groups present. Proper handling and safety measures should be observed when working with this substance in laboratory settings.

4-chloro-6,8-dimethyl-2-phenyl-quinoline

101602-31-7: 4-Chloro-6,8-dimethyl-2-phenyl-quinoline is a synthetic organic compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. This compound features a chlorine atom at the 4-position and two methyl groups at the 6 and 8 positions, along with a phenyl group at the 2-position, contributing to its unique chemical properties. The presence of these substituents can influence its reactivity, solubility, and potential biological activity. Typically, quinoline derivatives are known for their applications in pharmaceuticals, agrochemicals, and as dyes. The chlorine and methyl groups can enhance lipophilicity, potentially affecting the compound's interaction with biological systems. Additionally, the compound may exhibit fluorescence, making it useful in various analytical applications. As with many organic compounds, its stability, reactivity, and potential toxicity would depend on environmental conditions and specific functional groups present. Proper handling and safety measures should be observed when working with this substance in laboratory settings.

CAS 101602-31-7

4-chloro-6,8-dimethyl-2-phenyl-quinoline

QUINOLINE, 4-CHLORO-6,8-DIMETHYL-2-PHENYL-

Ref: IN-DA0004YQ

4-Chloro-6,8-dimethyl-2-phenylquinoline

Ref: 54-OR309307