(3-{[4-(Trifluoromethoxy)phenoxy]methyl}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 chemical reactions, including Suzuki coupling. The compound features a phenyl ring substituted with a trifluoromethoxy group, which enhances its electronic properties and solubility in organic solvents. The presence of the boronic acid moiety imparts acidity, allowing it to participate in acid-base reactions. This compound is typically used in organic synthesis, medicinal chemistry, and materials science due to its reactivity and ability to form complexes with biomolecules. Its trifluoromethoxy group can also influence its biological activity and interaction with other chemical entities. Overall, this compound exemplifies the versatility of boronic acids in synthetic applications and their role in developing new materials and pharmaceuticals.

(3-{[4-(trifluoromethoxy)phenoxy]methyl}phenyl)boronic acid

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3-((4'-(Trifluoromethoxy)phenoxy)methyl)phenylboronic acid

(3-((4-(Trifluoromethoxy)phenoxy)methyl)phenyl)boronic acid

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CAS 849062-06-2: (3-{[4-(trifluoromethoxy)phenoxy]methyl}phenyl)boronic acid

3-((4'-(Trifluoromethoxy)phenoxy)methyl)phenylboronic acid

Ref: 10-F623597

(3-((4-(Trifluoromethoxy)phenoxy)methyl)phenyl)boronic acid

Ref: IN-DA003HYX

3-((4'-(Trifluoromethoxy)phenoxy)methyl)phenylboronic acid

Ref: 54-PC412547

B-[3-[[4-(Trifluoromethoxy)phenoxy]methyl]phenyl]-Boronic acid

Ref: 3D-FT97058