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CAS 1451392-87-2

:

B-(6-Bromo-3-chloro-2-fluorophenyl)boronic acid

Description:
B-(6-Bromo-3-chloro-2-fluorophenyl)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 halogen atoms. The compound features a bromine atom at the 6-position, a chlorine atom at the 3-position, and a fluorine atom at the 2-position of the phenyl ring, contributing to its unique reactivity and properties. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. This compound may exhibit moderate solubility in polar solvents and can participate in various chemical reactions, including nucleophilic substitutions and coordination with metal catalysts. Its halogen substituents can influence its electronic properties and reactivity, making it a useful building block in the synthesis of pharmaceuticals and agrochemicals. As with many boronic acids, it is important to handle this compound with care due to potential reactivity and toxicity.
Formula:C6H4BBrClFO2
InChI:InChI=1S/C6H4BBrClFO2/c8-3-1-2-4(9)6(10)5(3)7(11)12/h1-2,11-12H
InChI key:InChIKey=RQWDCSBDDYTXMA-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(Cl)=CC=C1Br
Synonyms:
  • 2-Fluoro-3-chloro-6-bromophenylboronic acid
  • B-(6-Bromo-3-chloro-2-fluorophenyl)boronic acid
  • (6-Bromo-3-chloro-2-fluorophenyl)boronic acid
  • Boronic acid, B-(6-bromo-3-chloro-2-fluorophenyl)-
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