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CAS 352534-79-3

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2-Fluoro-5-formylbenzeneboronic acid

Description:
2-Fluoro-5-formylbenzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a formyl group attached to a fluorinated aromatic ring. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, owing to the presence of the boronic acid moiety. The fluorine atom introduces unique electronic properties, potentially enhancing its reactivity in various chemical reactions, including cross-coupling reactions and as a building block in organic synthesis. The boronic acid group allows for the formation of reversible covalent bonds with diols, making it useful in the development of sensors and drug delivery systems. Additionally, the compound may exhibit interesting biological activities, making it a candidate for further research in medicinal chemistry. Its reactivity and functional groups make it valuable in synthetic organic chemistry, particularly in the synthesis of complex molecules. As with all boronic acids, care should be taken in handling due to potential reactivity with moisture and other nucleophiles.
Formula:C7H6BFO3
InChI:InChI=1/C7H6BFO3/c9-7-2-1-5(4-10)3-6(7)8(11)12/h1-4,11-12H
SMILES:c1cc(c(cc1C=O)B(O)O)F
Synonyms:
  • (2-Fluoro-5-formylphenyl)boronic acid
  • Boronic acid, B-(2-fluoro-5-formylphenyl)-
  • 2-Fluoro-5-formylphenylboronic acid
  • 2-Fluoro-5-Formylphenylboronic
  • 2-FLUORO-5-FORMYLBENZENEBORONIC ACID
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