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CAS 193353-34-3

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2,5-Difluorobenzeneboronic acid

Description:
2,5-Difluorobenzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a benzene ring that has two fluorine substituents at the 2 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, which can engage in hydrogen bonding. The presence of fluorine atoms enhances the compound's reactivity and can influence its electronic properties, making it useful in various applications, including medicinal chemistry and materials science. Boronic acids are known for their ability to form reversible covalent bonds with diols, which is a key feature in applications such as drug delivery and sensor development. Additionally, 2,5-Difluorobenzeneboronic acid can serve as a building block in organic synthesis, particularly in Suzuki coupling reactions, which are widely used for the formation of carbon-carbon bonds. Its unique structure and reactivity make it a valuable compound in both research and industrial applications.
Formula:C6H5FN2O2
InChI:InChI=1/C6H5FN2O2/c1-4-2-3-8-6(7)5(4)9(10)11/h2-3H,1H3
Synonyms:
  • 2,5-Difluorophenylboronic acid
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