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CAS 248270-25-9

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3-Fluoro-4-formylbenzeneboronic acid

Description:
3-Fluoro-4-formylbenzeneboronic acid is an organic compound characterized by the presence of a boronic acid functional group, a formyl group, and a fluorine atom attached to a benzene ring. The molecular structure features a boron atom bonded to a hydroxyl group and an aryl group, which enhances its reactivity in various chemical reactions, particularly in Suzuki coupling reactions. The formyl group (-CHO) introduces an aldehyde functionality, making the compound useful in organic synthesis and as an intermediate in the preparation of more complex molecules. The fluorine atom contributes to the compound's electronic properties, potentially influencing its reactivity and solubility. This compound is typically used in medicinal chemistry and materials science due to its ability to form stable complexes with various substrates. Additionally, its boronic acid moiety allows for participation in cross-coupling reactions, making it valuable in the synthesis of pharmaceuticals and agrochemicals. As with many boronic acids, it is important to handle this compound with care, considering its potential reactivity and the need for appropriate storage conditions.
Formula:C7H6BFO3
InChI:InChI=1/C7H6BFO3/c9-7-3-6(8(11)12)2-1-5(7)4-10/h1-4,11-12H
SMILES:c1cc(cc(c1C=O)F)B(O)O
Synonyms:
  • 4-Borono-3-fluorobenzaldehyde
  • 3-Fluoro-4-formylphenylboronic acid
  • (3-Fluoro-4-Formylphenyl)Boronic Acid
  • 3-Fluoro-4-formylphenylboronicacid
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