7-Bromo-2-chloro-3-phenylquinoline is an organic compound characterized by its complex heterocyclic structure, which includes a quinoline backbone substituted with bromine and chlorine atoms, as well as a phenyl group. The presence of the bromine and chlorine substituents contributes to its reactivity and potential applications in various chemical reactions, such as electrophilic aromatic substitution. This compound typically exhibits moderate to high lipophilicity due to the aromatic nature of the quinoline and phenyl groups, which can influence its solubility in organic solvents. Additionally, the halogen substituents can enhance its biological activity, making it of interest in medicinal chemistry for potential pharmaceutical applications. The compound may also display fluorescence properties, which can be useful in analytical chemistry. Its synthesis and characterization often involve standard organic chemistry techniques, including nucleophilic substitution and coupling reactions. As with many halogenated compounds, safety precautions should be taken due to potential toxicity and environmental concerns associated with halogenated organic substances.

7-bromo-2-chloro-3-phenylquinoline

85274-44-8: 7-Bromo-2-chloro-3-phenylquinoline is an organic compound characterized by its complex heterocyclic structure, which includes a quinoline backbone substituted with bromine and chlorine atoms, as well as a phenyl group. The presence of the bromine and chlorine substituents contributes to its reactivity and potential applications in various chemical reactions, such as electrophilic aromatic substitution. This compound typically exhibits moderate to high lipophilicity due to the aromatic nature of the quinoline and phenyl groups, which can influence its solubility in organic solvents. Additionally, the halogen substituents can enhance its biological activity, making it of interest in medicinal chemistry for potential pharmaceutical applications. The compound may also display fluorescence properties, which can be useful in analytical chemistry. Its synthesis and characterization often involve standard organic chemistry techniques, including nucleophilic substitution and coupling reactions. As with many halogenated compounds, safety precautions should be taken due to potential toxicity and environmental concerns associated with halogenated organic substances.

CAS 85274-44-8

7-bromo-2-chloro-3-phenylquinoline

7-Bromo-2-chloro-3-phenylquinoline

Ref: 54-OR309274