[4-Chloro-3-(trifluoromethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a chlorine atom and a trifluoromethoxy group, which enhances its reactivity and solubility in organic solvents. The trifluoromethoxy group contributes to the compound's unique electronic properties, potentially influencing its reactivity and interactions with other molecules. This compound is typically used in medicinal chemistry and materials science, where boronic acids play a crucial role in drug development and the synthesis of complex organic molecules. Its stability and reactivity under various conditions make it a valuable intermediate in synthetic pathways. Safety data should be consulted for handling, as boronic acids can pose health risks if not managed properly.

[4-CHLORO-3-(TRIFLUOROMETHOXY)PHENYL]BORONIC ACID

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CAS 902757-07-7: [4-CHLORO-3-(TRIFLUOROMETHOXY)PHENYL]BORONIC ACID

(4-Chloro-3-(trifluoromethoxy)phenyl)boronic acid

Ref: 3D-CLB75707

Boronic acid, [4-chloro-3-(trifluoromethoxy)phenyl]-

Ref: IN-DA00IG2B

(4-Chloro-3-(trifluoromethoxy)phenyl)boronic acid

Ref: 54-PC102295

(4-Chloro-3-(trifluoromethoxy)phenyl)boronic acid

Ref: 10-F615502