4-Bromo-7-(trifluoromethyl)quinoline is a heterocyclic organic compound characterized by its quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 4-position and a trifluoromethyl group at the 7-position significantly influences its chemical properties and reactivity. This compound typically exhibits a pale yellow to brownish color and is sparingly soluble in water but more soluble in organic solvents such as dichloromethane and ethanol. Its molecular structure contributes to its potential applications in pharmaceuticals, agrochemicals, and materials science, particularly in the development of biologically active compounds. The trifluoromethyl group enhances lipophilicity and metabolic stability, making it a valuable moiety in drug design. Additionally, the compound may exhibit interesting electronic properties due to the presence of halogen substituents, which can affect its interaction with biological targets. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks.

4-bromo-7-(trifluoromethyl)quinoline

89446-67-3: 4-Bromo-7-(trifluoromethyl)quinoline is a heterocyclic organic compound characterized by its quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of a bromine atom at the 4-position and a trifluoromethyl group at the 7-position significantly influences its chemical properties and reactivity. This compound typically exhibits a pale yellow to brownish color and is sparingly soluble in water but more soluble in organic solvents such as dichloromethane and ethanol. Its molecular structure contributes to its potential applications in pharmaceuticals, agrochemicals, and materials science, particularly in the development of biologically active compounds. The trifluoromethyl group enhances lipophilicity and metabolic stability, making it a valuable moiety in drug design. Additionally, the compound may exhibit interesting electronic properties due to the presence of halogen substituents, which can affect its interaction with biological targets. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks.

CAS 89446-67-3

4-bromo-7-(trifluoromethyl)quinoline

4-Bromo-7-(trifluoromethyl)quinoline

Ref: IN-DA0088GB

4-Bromo-7-trifluoromethylquinoline

Ref: 54-PC404570

4-Bromo-7-(trifluoromethyl)quinoline

Ref: 10-F321191