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CAS 1451393-13-7

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B-(4-Chloro-2-fluoro-3-hydroxyphenyl)boronic acid

Description:
B-(4-Chloro-2-fluoro-3-hydroxyphenyl)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 chlorine, fluorine, and hydroxyl groups. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and alcohols, and possessing moderate stability under standard conditions. The presence of the boronic acid moiety allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The chlorine and fluorine substituents can influence the compound's electronic properties and reactivity, while the hydroxyl group can engage in hydrogen bonding, affecting solubility and interaction with biological targets. Overall, this compound's unique structural features contribute to its potential applications in pharmaceuticals and materials science.
Formula:C6H5BClFO3
InChI:InChI=1S/C6H5BClFO3/c8-4-2-1-3(7(11)12)5(9)6(4)10/h1-2,10-12H
InChI key:InChIKey=CYFLEBLGQHFBBB-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(O)=C(Cl)C=C1
Synonyms:
  • B-(4-Chloro-2-fluoro-3-hydroxyphenyl)boronic acid
  • 4-Chloro-2-fluoro-3-hydroxyphenylboronic acid
  • Boronic acid, B-(4-chloro-2-fluoro-3-hydroxyphenyl)-
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