8-(Trifluoromethoxy)quinolin-3-ol is a chemical compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a hydroxyl group (-OH) at the 3-position and a trifluoromethoxy group (-O-CF3) at the 8-position significantly influences its chemical properties and reactivity. This compound is typically a solid at room temperature and exhibits moderate solubility in organic solvents, while its solubility in water may be limited due to the hydrophobic nature of the trifluoromethoxy group. The trifluoromethoxy substituent enhances the compound's lipophilicity and can affect its biological activity, making it of interest in medicinal chemistry and drug development. Additionally, the presence of fluorine atoms can impart unique electronic properties, potentially influencing the compound's interaction with biological targets. Overall, 8-(trifluoromethoxy)quinolin-3-ol is notable for its potential applications in pharmaceuticals, particularly in the development of compounds with specific biological activities.

8-(trifluoromethoxy)quinolin-3-ol

1261886-64-9: 8-(Trifluoromethoxy)quinolin-3-ol is a chemical compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a hydroxyl group (-OH) at the 3-position and a trifluoromethoxy group (-O-CF3) at the 8-position significantly influences its chemical properties and reactivity. This compound is typically a solid at room temperature and exhibits moderate solubility in organic solvents, while its solubility in water may be limited due to the hydrophobic nature of the trifluoromethoxy group. The trifluoromethoxy substituent enhances the compound's lipophilicity and can affect its biological activity, making it of interest in medicinal chemistry and drug development. Additionally, the presence of fluorine atoms can impart unique electronic properties, potentially influencing the compound's interaction with biological targets. Overall, 8-(trifluoromethoxy)quinolin-3-ol is notable for its potential applications in pharmaceuticals, particularly in the development of compounds with specific biological activities.

CAS 1261886-64-9

8-(trifluoromethoxy)quinolin-3-ol

8-(trifluoromethoxy)quinolin-3-ol

Ref: IN-DA01FPSI

8-(Trifluoromethoxy)quinolin-3-ol

Ref: 54-PC102669

8-(TRIFLUOROMETHOXY)QUINOLIN-3-OL

Ref: 10-F816734