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CAS 1238196-66-1

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4-Chloro-2-hydroxyphenylboronic acid

Description:
4-Chloro-2-hydroxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenolic structure. This compound features a chlorine atom and a hydroxyl group on the aromatic ring, which contribute to its reactivity and solubility properties. It is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, making it useful in various chemical reactions. The boronic acid moiety allows for the formation of covalent bonds with diols, which is particularly valuable in organic synthesis and medicinal chemistry, especially in the development of pharmaceuticals. Additionally, this compound can participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Its unique structural features and reactivity profile make it a significant intermediate in the synthesis of complex organic molecules. Safety precautions should be observed when handling this compound, as with many organoboron compounds, due to potential toxicity and environmental concerns.
Formula:C6H6BClO3
InChI:InChI=1S/C6H6BClO3/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,9-11H
InChI key:InChIKey=XBNRJKSGOLRSRX-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(O)C=C(Cl)C=C1
Synonyms:
  • 4-Chloro-2-hydroxyphenylboronic acid
  • 2-Hydroxy-4-chlorophenylboronic acid
  • B-(4-Chloro-2-hydroxyphenyl)boronic acid
  • Boronic acid, B-(4-chloro-2-hydroxyphenyl)-
  • EOS-60945
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