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CAS 870777-22-3

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B-(2-Fluoro-6-iodophenyl)boronic acid

Description:
B-(2-Fluoro-6-iodophenyl)boronic 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 properties associated with boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the fluorine and iodine substituents can influence its reactivity, solubility, and biological activity. Generally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the unique halogen substituents may enhance the compound's potential as a ligand in coordination chemistry or as a building block in the development of pharmaceuticals. Its specific characteristics, such as melting point, solubility, and stability, would depend on the molecular structure and the conditions under which it is handled.
Formula:C6H5BFIO2
InChI:InChI=1S/C6H5BFIO2/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3,10-11H
InChI key:InChIKey=LBSXGVJFWVWITH-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C=CC=C1I
Synonyms:
  • B-(2-Fluoro-6-iodophenyl)boronic acid
  • Boronic acid, B-(2-fluoro-6-iodophenyl)-
  • Boronic acid, (2-fluoro-6-iodophenyl)-
  • 2-Fluoro-6-iodophenylboronic acid
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