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CAS 226396-32-3

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2,3,4-Trifluorophenylboronic acid

Description:
2,3,4-Trifluorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has three fluorine substituents at the 2, 3, and 4 positions. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the boronic acid group. The trifluoromethyl groups enhance its reactivity and influence its electronic properties, making it useful in various chemical applications, including cross-coupling reactions in organic synthesis and as a building block in the development of pharmaceuticals. The presence of fluorine atoms can also impart unique characteristics, such as increased lipophilicity and altered biological activity. Additionally, 2,3,4-trifluorophenylboronic acid can participate in reversible covalent bonding with diols, which is significant in the design of sensors and drug delivery systems. Overall, this compound is valuable in both academic research and industrial applications due to its versatile reactivity and functional properties.
Formula:C6H4BF3O2
InChI:InChI=1/C6H4BF3O2/c8-4-2-1-3(7(11)12)5(9)6(4)10/h1-2,11-12H
SMILES:c1cc(c(c(c1B(O)O)F)F)F
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