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CAS 2096341-70-5

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B-[5-Bromo-2-fluoro-3-(trifluoromethyl)phenyl]boronic acid

Description:
B-[5-Bromo-2-fluoro-3-(trifluoromethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a bromine atom, a fluorine atom, and a trifluoromethyl group, contributing to its unique electronic and steric properties. The presence of these halogen substituents can enhance the compound's reactivity and influence its interactions in various chemical environments. Boronic acids are typically polar and can exhibit solubility in polar solvents, making them versatile in various applications, including cross-coupling reactions and as intermediates in the synthesis of pharmaceuticals. Additionally, the trifluoromethyl group is known to impart lipophilicity, which can affect the compound's biological activity and pharmacokinetics. Overall, this compound's distinctive structure and functional groups make it a valuable entity in chemical research and development.
Formula:C7H4BBrF4O2
InChI:InChI=1S/C7H4BBrF4O2/c9-3-1-4(7(11,12)13)6(10)5(2-3)8(14)15/h1-2,14-15H
InChI key:InChIKey=WRIJOUMGMHQBFI-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(F)C(B(O)O)=CC(Br)=C1
Synonyms:
  • B-[5-Bromo-2-fluoro-3-(trifluoromethyl)phenyl]boronic acid
  • Boronic acid, B-[5-bromo-2-fluoro-3-(trifluoromethyl)phenyl]-
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