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CAS 913835-71-9

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B-(2-Chloro-5-hydroxyphenyl)boronic acid

Description:
B-(2-Chloro-5-hydroxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that features both a chlorine atom and a hydroxyl group. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with moderate solubility in polar solvents like water and alcohols, due to the presence of the boronic acid group. It is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The chlorine substituent can influence the compound's reactivity and biological activity, while the hydroxyl group can participate in hydrogen bonding, enhancing its solubility and interaction with biological molecules. B-(2-Chloro-5-hydroxyphenyl)boronic acid is often utilized in the development of pharmaceuticals and as a reagent in cross-coupling reactions, highlighting its significance in both academic research and industrial applications.
Formula:C6H6BClO3
InChI:InChI=1S/C6H6BClO3/c8-6-2-1-4(9)3-5(6)7(10)11/h1-3,9-11H
InChI key:InChIKey=SLAPQAZQRNMJLC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C=CC(O)=C1
Synonyms:
  • Boronic acid, B-(2-chloro-5-hydroxyphenyl)-
  • B-(2-Chloro-5-hydroxyphenyl)boronic acid
  • 2-Chloro-5-hydroxyphenylboronic acid
  • Boronic acid, (2-chloro-5-hydroxyphenyl)-
  • 2-Chloro-5-hydroxybenzeneboronic acid
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