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CAS 179923-32-1

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2,3,4,5-Tetrafluorobenzeneboronic acid

Description:
2,3,4,5-Tetrafluorobenzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a benzene ring that has four fluorine substituents. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The presence of fluorine atoms enhances its reactivity and stability, making it useful in various chemical applications, including organic synthesis and materials science. It can participate in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds. Additionally, the fluorinated structure may impart unique electronic properties, making it valuable in the development of pharmaceuticals and agrochemicals. Safety considerations should be taken into account when handling this compound, as boronic acids can be irritants, and the fluorinated nature may pose specific environmental concerns. Overall, 2,3,4,5-Tetrafluorobenzeneboronic acid is a versatile reagent in modern organic chemistry.
Formula:C6H3BF4O2
InChI:InChI=1/C6H3BF4O2/c8-3-1-2(7(12)13)4(9)6(11)5(3)10/h1,12-13H
SMILES:c1c(c(c(c(c1F)F)F)F)B(O)O
Synonyms:
  • 2,3,4,5-Tetrafluorophenylboronic acid
  • 2,3,4,5-
  • BORONIC ACID,B-(2,3,4,5-TETRAFLUOROPHENYL)-
  • Tetrafluorophenylboronic acid
  • 2,3,4,5-TETRAFLUOROBENZENEBORONIC ACID
  • 2,3,4,5-tetrafluorobenzeneboronic acid 97%
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