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CAS 866683-41-2

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2-Fluoro-5-iodophenylboronic acid

Description:
2-Fluoro-5-iodophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both a fluorine and an iodine atom. 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 boronic acid group, which can form hydrogen bonds. The presence of the fluorine and iodine substituents can influence its reactivity and stability, making it useful in various chemical reactions, particularly in Suzuki coupling reactions for the synthesis of biaryl compounds. Additionally, the boronic acid moiety allows for the formation of reversible complexes with diols, which is significant in biological applications and sensor development. Its unique combination of halogen substituents may also impart specific electronic properties, making it a candidate for studies in materials science and medicinal chemistry. As with many organoboron compounds, care should be taken in handling due to potential reactivity and toxicity.
Formula:C6H5BFIO2
InChI:InChI=1S/C6H5BFIO2/c8-6-2-1-4(9)3-5(6)7(10)11/h1-3,10-11H
InChI key:InChIKey=QZPDCZSOVJLEKB-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C=CC(I)=C1
Synonyms:
  • B-(2-Fluoro-5-iodophenyl)boronic acid
  • Boronic acid, B-(2-fluoro-5-iodophenyl)-
  • 2-Fluoro-5-iodophenylboronic acid
  • Boronic acid, (2-fluoro-5-iodophenyl)-
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