8-Bromo-5-(trifluoromethyl)quinoline is a chemical compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. The presence of a bromine atom at the 8-position and a trifluoromethyl group at the 5-position significantly influences its chemical properties and reactivity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The bromine substituent can participate in electrophilic aromatic substitution reactions, while the trifluoromethyl group enhances the compound's lipophilicity and can affect its electronic properties, making it a useful moiety in medicinal chemistry and material science. Additionally, the presence of fluorine atoms often imparts unique characteristics such as increased metabolic stability and altered biological activity. As with many halogenated compounds, safety precautions should be taken due to potential toxicity and environmental concerns. Overall, 8-bromo-5-(trifluoromethyl)quinoline is of interest in various fields, including pharmaceuticals and agrochemicals.

8-bromo-5-(trifluoromethyl)quinoline

917251-92-4: 8-Bromo-5-(trifluoromethyl)quinoline is a chemical compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. The presence of a bromine atom at the 8-position and a trifluoromethyl group at the 5-position significantly influences its chemical properties and reactivity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The bromine substituent can participate in electrophilic aromatic substitution reactions, while the trifluoromethyl group enhances the compound's lipophilicity and can affect its electronic properties, making it a useful moiety in medicinal chemistry and material science. Additionally, the presence of fluorine atoms often imparts unique characteristics such as increased metabolic stability and altered biological activity. As with many halogenated compounds, safety precautions should be taken due to potential toxicity and environmental concerns. Overall, 8-bromo-5-(trifluoromethyl)quinoline is of interest in various fields, including pharmaceuticals and agrochemicals.

CAS 917251-92-4

8-bromo-5-(trifluoromethyl)quinoline

8-Bromo-5-(trifluoromethyl)quinoline

Ref: IN-DA00H1V6

8-Bromo-5-(trifluoromethyl)quinoline

Ref: 54-PC103672

8-Bromo-5-(trifluoromethyl)quinoline

Ref: 10-F323681