4-Chloro-7-(trifluoromethoxy)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 chlorine atom at the 4-position and a trifluoromethoxy group at the 7-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. Its trifluoromethoxy group contributes to its lipophilicity and can enhance biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The chlorine substituent can also affect the compound's electronic properties and potential interactions with biological targets. Additionally, 4-chloro-7-(trifluoromethoxy)quinoline may exhibit specific spectral characteristics in techniques such as NMR and IR spectroscopy, which can be utilized for its identification and analysis. Overall, this compound's unique structural features make it a subject of interest in various chemical research fields.

4-chloro-7-(trifluoromethoxy)quinoline

40516-31-2: 4-Chloro-7-(trifluoromethoxy)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 chlorine atom at the 4-position and a trifluoromethoxy group at the 7-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. Its trifluoromethoxy group contributes to its lipophilicity and can enhance biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The chlorine substituent can also affect the compound's electronic properties and potential interactions with biological targets. Additionally, 4-chloro-7-(trifluoromethoxy)quinoline may exhibit specific spectral characteristics in techniques such as NMR and IR spectroscopy, which can be utilized for its identification and analysis. Overall, this compound's unique structural features make it a subject of interest in various chemical research fields.

CAS 40516-31-2

4-chloro-7-(trifluoromethoxy)quinoline

4-Chloro-7-(trifluoromethoxy)quinoline

Ref: IN-DA00C70V

4-Chloro-7-(trifluoromethoxy)quinoline

Ref: 54-PC28306

4-Chloro-7-(trifluoromethoxy)quinoline

Ref: 10-F640329