3-(Trifluoromethyl)quinoline is an organic compound characterized by its quinoline backbone, which is a bicyclic structure composed of a benzene ring fused to a pyridine ring. The presence of a trifluoromethyl group (-CF3) at the 3-position of the quinoline significantly influences its chemical properties, enhancing its lipophilicity and potentially altering its reactivity and biological activity. This compound is typically a pale yellow to light brown solid at room temperature and is known for its stability under various conditions. It is often utilized in pharmaceutical research and development due to its potential as a building block in the synthesis of biologically active molecules. The trifluoromethyl group can also impart unique electronic properties, making it a valuable substituent in medicinal chemistry. Additionally, 3-(trifluoromethyl)quinoline may exhibit interesting photophysical properties, which can be exploited in various applications, including fluorescence-based assays. As with many fluorinated compounds, it is essential to handle it with care due to potential environmental and health impacts.

3-(trifluoromethyl)quinoline

25199-76-2: 3-(Trifluoromethyl)quinoline is an organic compound characterized by its quinoline backbone, which is a bicyclic structure composed of a benzene ring fused to a pyridine ring. The presence of a trifluoromethyl group (-CF3) at the 3-position of the quinoline significantly influences its chemical properties, enhancing its lipophilicity and potentially altering its reactivity and biological activity. This compound is typically a pale yellow to light brown solid at room temperature and is known for its stability under various conditions. It is often utilized in pharmaceutical research and development due to its potential as a building block in the synthesis of biologically active molecules. The trifluoromethyl group can also impart unique electronic properties, making it a valuable substituent in medicinal chemistry. Additionally, 3-(trifluoromethyl)quinoline may exhibit interesting photophysical properties, which can be exploited in various applications, including fluorescence-based assays. As with many fluorinated compounds, it is essential to handle it with care due to potential environmental and health impacts.

CAS 25199-76-2

3-(trifluoromethyl)quinoline

3-(Trifluoromethyl)quinoline

Ref: IN-DA002QV6

3-(Trifluoromethyl)quinoline

Ref: 54-PC906529

3-(Trifluoromethyl)quinoline

Ref: 10-F036010