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CAS 511295-00-4

:

2,3,4,6-Tetrafluorobenzeneboronic acid

Description:
2,3,4,6-Tetrafluorobenzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a benzene ring that is substituted with four fluorine atoms. This compound typically exhibits a high degree of reactivity due to the boronic acid moiety, which can participate in various chemical reactions, including Suzuki coupling and other cross-coupling reactions, making it valuable in organic synthesis and materials science. The presence of fluorine atoms enhances its electronic properties, potentially increasing its lipophilicity and altering its reactivity compared to non-fluorinated analogs. Additionally, the fluorine substituents can influence the compound's solubility and stability in different solvents. 2,3,4,6-Tetrafluorobenzeneboronic acid is often used in the development of pharmaceuticals and agrochemicals, as well as in the synthesis of complex organic molecules. Safety data should be consulted when handling this compound, as boronic acids can be sensitive to moisture and may require specific storage conditions.
Formula:C6H3BF4O2
InChI:InChI=1/C6H3BF4O2/c8-2-1-3(9)5(10)6(11)4(2)7(12)13/h1,12-13H
SMILES:c1c(c(c(c(c1F)F)F)B(O)O)F
Synonyms:
  • (2,3,4,6-Tetrafluorophenyl)boronic acid
  • boronic acid, B-(2,3,4,6-tetrafluorophenyl)-
  • 2,3,4,6-Tetrafluorophenylboronicacid
  • 2,3,4,6-Tetrafluorophenylboronic acid:
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