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CAS 143418-49-9

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(3,4,5-Trifluorophenyl)boronic acid

Description:
(3,4,5-Trifluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that has three fluorine substituents at the 3, 4, and 5 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 polarity, making it useful in various chemical reactions, particularly in Suzuki coupling reactions for the formation of carbon-carbon bonds. Its unique electronic properties, influenced by the electronegative fluorine atoms, can also affect its behavior in biological systems and materials science applications. Additionally, (3,4,5-Trifluorophenyl)boronic acid is often utilized in the synthesis of pharmaceuticals and agrochemicals, as well as in the development of sensors and catalysts. Proper handling and storage are essential due to its potential reactivity and the need for safety precautions when working with boronic acids.
Formula:C6H4BF3O2
InChI:InChI=1S/C6H4BF3O2/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2,11-12H
InChI key:InChIKey=UHDDEIOYXFXNNJ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(F)=C(F)C(F)=C1
Synonyms:
  • 3,4,5-Trifluorobenzeneboronic Acid
  • 3,4,5-Trifluorophenyl boronic acid
  • Alkaneboronic
  • B-(3,4,5-Trifluorophenyl)boronic acid
  • Boronic acid, (3,4,5-trifluorophenyl)-
  • Boronic acid, B-(3,4,5-trifluorophenyl)-
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