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CAS 374538-01-9

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4-Fluoro-3-formylbenzeneboronic acid

Description:
4-Fluoro-3-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. The molecular structure features a benzene ring substituted with a fluorine atom at the para position relative to the boronic acid group and an aldehyde (formyl) group at the meta position. This compound is typically used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in cross-coupling reactions, such as Suzuki-Miyaura coupling. The boronic acid moiety allows for the formation of stable complexes with diols, making it useful in various applications, including sensor technology and material science. Additionally, the presence of the fluorine atom can enhance the compound's biological activity and lipophilicity. As with many boronic acids, it is important to handle this compound with care, as it may be sensitive to moisture and can undergo hydrolysis in aqueous environments.
Formula:C7H6BFO3
InChI:InChI=1/C7H6BFO3/c9-7-2-1-6(8(11)12)3-5(7)4-10/h1-4,11-12H
SMILES:c1cc(c(cc1B(O)O)C=O)F
Synonyms:
  • 5-Borono-2-fluorobenzaldehyde
  • 4-Fluoro-3-formylphenylboronic acid
  • (4-Fluoro-3-Formylphenyl)Boronic Acid
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