4-Bromo-2-(trifluoromethyl)quinoline is an organic compound characterized by its quinoline backbone, which is a bicyclic structure consisting of a benzene ring fused to a pyridine ring. The presence of a bromine atom at the 4-position and a trifluoromethyl group at the 2-position significantly influences its chemical properties and reactivity. This compound is typically a solid at room temperature and exhibits moderate solubility in organic solvents. The trifluoromethyl group is known for imparting unique electronic properties, enhancing lipophilicity, and influencing biological activity. As a halogenated compound, it may exhibit interesting reactivity patterns, including potential electrophilic substitution reactions. 4-Bromo-2-(trifluoromethyl)quinoline may also be of interest in medicinal chemistry due to its potential biological activities, including antimicrobial or antitumor properties. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, this compound serves as a valuable building block in organic synthesis and pharmaceutical development.

4-bromo-2-(trifluoromethyl)quinoline

18706-25-7: 4-Bromo-2-(trifluoromethyl)quinoline is an organic compound characterized by its quinoline backbone, which is a bicyclic structure consisting of a benzene ring fused to a pyridine ring. The presence of a bromine atom at the 4-position and a trifluoromethyl group at the 2-position significantly influences its chemical properties and reactivity. This compound is typically a solid at room temperature and exhibits moderate solubility in organic solvents. The trifluoromethyl group is known for imparting unique electronic properties, enhancing lipophilicity, and influencing biological activity. As a halogenated compound, it may exhibit interesting reactivity patterns, including potential electrophilic substitution reactions. 4-Bromo-2-(trifluoromethyl)quinoline may also be of interest in medicinal chemistry due to its potential biological activities, including antimicrobial or antitumor properties. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, this compound serves as a valuable building block in organic synthesis and pharmaceutical development.

4-Bromo-2-(trifluoromethyl)quinoline

<p>4-Bromo-2-(trifluoromethyl)quinoline</p>

CAS 18706-25-7

4-bromo-2-(trifluoromethyl)quinoline

4-Bromo-2-(trifluoromethyl)quinoline

Ref: IN-DA00754C

4-Bromo-2-(trifluoromethyl)quinoline

Ref: 54-PC49117

4-Bromo-2-(trifluoromethyl)quinoline

Ref: 10-F223359