6-Bromo-2-chloro-3-phenylquinoline is a heterocyclic organic compound characterized by its quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of bromine and chlorine substituents at the 6 and 2 positions, respectively, introduces significant reactivity and influences its chemical properties. This compound typically exhibits a pale yellow to brownish color and is sparingly soluble in water but more soluble in organic solvents like ethanol and dichloromethane. Its structure allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with quinoline derivatives. The compound may also exhibit fluorescence properties, making it useful in various analytical applications. Additionally, the presence of halogens can enhance its reactivity in electrophilic substitution reactions, making it a valuable intermediate in organic synthesis. Safety data should be consulted, as halogenated compounds can pose health risks, and appropriate handling and disposal procedures should be followed.

6-bromo-2-chloro-3-phenylquinoline

85274-48-2: 6-Bromo-2-chloro-3-phenylquinoline is a heterocyclic organic compound characterized by its quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of bromine and chlorine substituents at the 6 and 2 positions, respectively, introduces significant reactivity and influences its chemical properties. This compound typically exhibits a pale yellow to brownish color and is sparingly soluble in water but more soluble in organic solvents like ethanol and dichloromethane. Its structure allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with quinoline derivatives. The compound may also exhibit fluorescence properties, making it useful in various analytical applications. Additionally, the presence of halogens can enhance its reactivity in electrophilic substitution reactions, making it a valuable intermediate in organic synthesis. Safety data should be consulted, as halogenated compounds can pose health risks, and appropriate handling and disposal procedures should be followed.

CAS 85274-48-2

6-bromo-2-chloro-3-phenylquinoline

6-Bromo-2-chloro-3-phenylquinoline

Ref: 54-OR309271