4-Chloro-6-(trifluoromethoxy)-2-(trifluoromethyl)quinoline is a synthetic organic compound belonging to the quinoline class, characterized by its complex structure that includes both chloro and trifluoromethyl groups. This compound features a quinoline backbone, which is a bicyclic structure composed of a benzene ring fused to a pyridine ring. The presence of the chloro group at the 4-position and the trifluoromethoxy and trifluoromethyl substituents at the 6 and 2 positions, respectively, significantly influence its chemical properties, including its reactivity and polarity. The trifluoromethyl groups enhance the lipophilicity and may contribute to biological activity, making this compound of interest in medicinal chemistry and material science. Additionally, the trifluoromethoxy group can impart unique electronic properties, potentially affecting the compound's interaction with biological targets. Overall, this compound's unique substituents suggest potential applications in pharmaceuticals or agrochemicals, although specific biological activities would require further investigation.

4-chloro-6-(trifluoromethoxy)-2-(trifluoromethyl)quinoline

503148-24-1: 4-Chloro-6-(trifluoromethoxy)-2-(trifluoromethyl)quinoline is a synthetic organic compound belonging to the quinoline class, characterized by its complex structure that includes both chloro and trifluoromethyl groups. This compound features a quinoline backbone, which is a bicyclic structure composed of a benzene ring fused to a pyridine ring. The presence of the chloro group at the 4-position and the trifluoromethoxy and trifluoromethyl substituents at the 6 and 2 positions, respectively, significantly influence its chemical properties, including its reactivity and polarity. The trifluoromethyl groups enhance the lipophilicity and may contribute to biological activity, making this compound of interest in medicinal chemistry and material science. Additionally, the trifluoromethoxy group can impart unique electronic properties, potentially affecting the compound's interaction with biological targets. Overall, this compound's unique substituents suggest potential applications in pharmaceuticals or agrochemicals, although specific biological activities would require further investigation.

CAS 503148-24-1

4-chloro-6-(trifluoromethoxy)-2-(trifluoromethyl)quinoline

4-Chloro-6-(trifluoromethoxy)-2-(trifluoromethyl)quinoline

Ref: IN-DA00DHU0

4-Chloro-6-(trifluoromethoxy)-2-(trifluoromethyl)quinoline

Ref: 54-PC31863