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CAS 352535-84-3

:

B-(3-Bromo-2,6-difluorophenyl)boronic acid

Description:
B-(3-Bromo-2,6-difluorophenyl)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 bromine and fluorine atoms. 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 bromine and fluorine substituents can influence its reactivity, solubility, and electronic properties, potentially enhancing its utility in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. Additionally, the fluorine atoms may impart unique characteristics such as increased lipophilicity or altered biological activity. As with many boronic acids, it is important to handle this compound with care, as it may be sensitive to moisture and can undergo hydrolysis. Overall, B-(3-Bromo-2,6-difluorophenyl)boronic acid serves as a valuable building block in the synthesis of more complex organic molecules.
Formula:C6H4BBrF2O2
InChI:InChI=1S/C6H4BBrF2O2/c8-3-1-2-4(9)5(6(3)10)7(11)12/h1-2,11-12H
InChI key:InChIKey=IOPHTXLBAFNMMI-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(Br)=CC=C1F
Synonyms:
  • 3-Bromo-2 6-Difluorophenylboronic Acid
  • 3-Bromo-2,6-difluorophenylboronic acid
  • B-(3-Bromo-2,6-difluorophenyl)boronic acid
  • Boronic acid, (3-bromo-2,6-difluorophenyl)-
  • boronic acid, B-(3-bromo-2,6-difluorophenyl)-
  • (3-Bromo-2,6-difluorophenyl)boronic acid
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