4,7-Dichloro-8-methyl-2-(trifluoromethyl)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 two chlorine atoms at the 4 and 7 positions, a methyl group at the 8 position, and a trifluoromethyl group at the 2 position, contributing to its unique chemical properties. The presence of halogen substituents enhances its reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The trifluoromethyl group is particularly notable for imparting lipophilicity and influencing the compound's biological activity. This compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential uses in medicinal chemistry, particularly in the development of antimicrobial or anticancer agents, although specific biological activities would require further investigation. Safety data should be consulted for handling and usage, as halogenated compounds can pose environmental and health risks.

4,7-dichloro-8-methyl-2-(trifluoromethyl)quinoline

887350-78-9: 4,7-Dichloro-8-methyl-2-(trifluoromethyl)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 two chlorine atoms at the 4 and 7 positions, a methyl group at the 8 position, and a trifluoromethyl group at the 2 position, contributing to its unique chemical properties. The presence of halogen substituents enhances its reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The trifluoromethyl group is particularly notable for imparting lipophilicity and influencing the compound's biological activity. This compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential uses in medicinal chemistry, particularly in the development of antimicrobial or anticancer agents, although specific biological activities would require further investigation. Safety data should be consulted for handling and usage, as halogenated compounds can pose environmental and health risks.

CAS 887350-78-9

4,7-dichloro-8-methyl-2-(trifluoromethyl)quinoline

4,7-Dichloro-8-methyl-2-(trifluoromethyl)quinoline

Ref: IN-DA003KK5

4,7-Dichloro-8-methyl-2-(trifluoromethyl)quinoline

Ref: 10-F215933