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CAS 870778-85-1

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(2-fluoro-3,5-diformylphenyl)boronic acid

Description:
(2-Fluoro-3,5-diformylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a substituted phenyl ring. The compound features a fluorine atom at the 2-position and two formyl groups at the 3 and 5 positions of the phenyl ring, which contribute to its reactivity and potential applications in organic synthesis and materials science. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various chemical reactions, including Suzuki coupling reactions. The presence of the formyl groups enhances the compound's electrophilicity, allowing for further functionalization. Additionally, the fluorine substitution can influence the compound's electronic properties and solubility. Overall, (2-fluoro-3,5-diformylphenyl)boronic acid is a versatile building block in organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, as well as in the synthesis of complex organic molecules.
Formula:C8H6BFO4
InChI:InChI=1/C8H6BFO4/c10-8-6(4-12)1-5(3-11)2-7(8)9(13)14/h1-4,13-14H
SMILES:c1c(cc(c(c1C=O)F)B(O)O)C=O
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