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CAS 313545-32-3

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2-Chloro-6-fluorophenylboronic acid

Description:
2-Chloro-6-fluorophenylboronic 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 chlorine and a fluorine atom. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, which is a characteristic feature of boronic acids due to their ability to form hydrogen bonds. The presence of the chlorine and fluorine substituents can influence its reactivity and interactions, making it useful in various chemical applications, including medicinal chemistry and organic synthesis. Boronic acids are known for their ability to form reversible complexes with diols, which is significant in the development of sensors and in the field of drug discovery. Additionally, 2-chloro-6-fluorophenylboronic acid may serve as a building block in the synthesis of more complex molecules, particularly in the context of Suzuki-Miyaura cross-coupling reactions. Its unique properties make it a valuable compound in both research and industrial applications.
Formula:C6H5BClFO2
InChI:InChI=1S/C6H5BClFO2/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3,10-11H
InChI key:InChIKey=NXSZSZJWZVLHAY-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C=CC=C1F
Synonyms:
  • 2-Chloro-6-fluorobenzeneboronic acid
  • 2-Chloro-6-fluorophenylboronic acid
  • B-(2-Chloro-6-fluorophenyl)boronic acid
  • Boronic acid, (2-chloro-6-fluorophenyl)-
  • Boronicacid, (2-chloro-6-fluorophenyl)- (9CI)
  • Boronic acid, B-(2-chloro-6-fluorophenyl)-
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