2,3,5-Trifluorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a trifluorinated phenyl ring. This compound typically exhibits a white to off-white crystalline solid form. The trifluoromethyl groups on the phenyl ring enhance its reactivity and solubility in polar solvents, making it useful in various chemical reactions, particularly in Suzuki coupling reactions for the synthesis of biaryl compounds. The boronic acid moiety allows for the formation of reversible complexes with diols, which is significant in applications such as drug delivery and sensor development. Additionally, the presence of fluorine atoms can impart unique electronic properties, influencing the compound's reactivity and stability. 2,3,5-Trifluorophenylboronic acid is often utilized in medicinal chemistry and materials science due to its ability to participate in cross-coupling reactions and its potential role in the development of fluorinated pharmaceuticals. Safety precautions should be observed when handling this compound, as with all boronic acids, due to potential irritant properties.

2,3,5-Trifluorophenylboronic acid

247564-73-4: 2,3,5-Trifluorobenzeneboronic acid, B-(2,3,5-Trifluorophenyl)boronic acid, Boronic acid, (2,3,5-trifluorophenyl)-, Boronic acid, B-(2,3,5-trifluorophenyl)-, 2,3,5-Trifluorophenylboronic acid

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CAS 247564-73-4: 2,3,5-Trifluorophenylboronic acid

2,3,5-Trifluorophenylboronic acid

Ref: 10-F218912

2,3,5-Trifluorophenylboronic acid

Ref: 3D-FT98577

Boronic acid, B-(2,3,5-trifluorophenyl)-

Ref: IN-DA002PC5

2,3,5-Trifluorobenzeneboronic acid

Ref: 54-PC1511

2,3,5-Trifluorophenylboronic Acid (contains varying amounts of Anhydride)

Ref: 3B-T2874