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CAS 247564-72-3

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(2,4,5-Trifluorophenyl)boronic acid

Description:
(2,4,5-Trifluorophenyl)boronic 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, 4, and 5 positions. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. The presence of fluorine atoms enhances its reactivity and stability, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in the synthesis of biaryl compounds. The boronic acid group allows for the formation of reversible complexes with diols, which is significant in applications such as drug delivery and sensor technology. Additionally, (2,4,5-Trifluorophenyl)boronic acid can exhibit unique electronic properties due to the electronegative fluorine atoms, influencing its behavior in chemical reactions and interactions with biological systems. Its applications extend to materials science and medicinal chemistry, where it serves as a building block for more complex molecules.
Formula:C6H4BF3O2
InChI:InChI=1/C6H4BF3O2/c8-4-2-6(10)5(9)1-3(4)7(11)12/h1-2,11-12H
InChI key:InChIKey=KCHHKNCSISEAAE-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C=C(F)C(F)=C1
Synonyms:
  • (2,4,5-Trifluorophenyl)boronic acid
  • 2,4,5-Trifluorophenylboronic acid
  • B-(2,4,5-Trifluorophenyl)boronic acid
  • Boronic acid, (2,4,5-trifluorophenyl)-
  • Boronic acid, B-(2,4,5-trifluorophenyl)-
  • RARECHEM AH PB 0119
  • 2,4,5-TRIFLUOROBENZENEBORONIC ACID
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