2,4-Dichloro-6-fluoro-3-phenylquinoline 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 two chlorine atoms and one fluorine atom at specific positions on the quinoline ring, contributing to its unique reactivity and potential biological activity. The presence of the phenyl group enhances its lipophilicity, which may influence its solubility and interaction with biological systems. Typically, compounds like this may exhibit antimicrobial, antiviral, or anticancer properties, making them of interest in medicinal chemistry. Its molecular structure allows for various substitution patterns, which can affect its pharmacokinetics and pharmacodynamics. Additionally, the compound's stability, melting point, and solubility in different solvents can vary based on its specific functional groups and overall molecular configuration. As with many halogenated compounds, it is essential to consider environmental and safety aspects during handling and application.

2,4-dichloro-6-fluoro-3-phenylquinoline

274691-28-0: 2,4-Dichloro-6-fluoro-3-phenylquinoline 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 two chlorine atoms and one fluorine atom at specific positions on the quinoline ring, contributing to its unique reactivity and potential biological activity. The presence of the phenyl group enhances its lipophilicity, which may influence its solubility and interaction with biological systems. Typically, compounds like this may exhibit antimicrobial, antiviral, or anticancer properties, making them of interest in medicinal chemistry. Its molecular structure allows for various substitution patterns, which can affect its pharmacokinetics and pharmacodynamics. Additionally, the compound's stability, melting point, and solubility in different solvents can vary based on its specific functional groups and overall molecular configuration. As with many halogenated compounds, it is essential to consider environmental and safety aspects during handling and application.

CAS 274691-28-0

2,4-dichloro-6-fluoro-3-phenylquinoline

2,4-Dichloro-6-fluoro-3-phenylquinoline

Ref: 54-PC31908