2-Chloro-6-(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 2-position and a trifluoromethoxy group at the 6-position significantly influences its chemical properties and reactivity. This compound is typically a pale yellow solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The trifluoromethoxy group enhances lipophilicity and can improve the compound's ability to penetrate biological membranes. Additionally, the chlorine substituent can affect the compound's electronic properties and reactivity, making it a valuable intermediate in organic synthesis. Its unique structure and functional groups may also contribute to its interactions with biological targets, making it of interest in drug discovery and development. As with many halogenated compounds, safety and handling precautions are essential due to potential toxicity and environmental impact.

2-chloro-6-(trifluoromethoxy) quinoline

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CAS 577967-67-0: 2-chloro-6-(trifluoromethoxy) quinoline

2-Chloro-6-(trifluoromethoxy)quinoline

Ref: IN-DA00EFSX

2-Chloro-6-(trifluoromethoxy)quinoline

Ref: 3D-CYA96767

2-CHLORO-6-(TRIFLUOROMETHOXY)QUINOLINE

Ref: 10-F845482

2-Chloro-6-(trifluoromethoxy)quinoline

Ref: 54-PC102792