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CAS 1256346-44-7

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B-(2,4-Dichloro-5-hydroxyphenyl)boronic acid

Description:
B-(2,4-Dichloro-5-hydroxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenolic ring that is substituted with two chlorine atoms and a hydroxyl group. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with solubility in polar solvents like water and alcohols due to the boronic acid moiety. It is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in medicinal chemistry. The presence of chlorine substituents can influence its reactivity and biological activity, potentially enhancing its efficacy in certain chemical reactions or biological interactions. Additionally, boronic acids are often utilized in the development of sensors and in the field of materials science for creating functionalized surfaces. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C6H5BCl2O3
InChI:InChI=1S/C6H5BCl2O3/c8-4-2-5(9)6(10)1-3(4)7(11)12/h1-2,10-12H
InChI key:InChIKey=QGQYVVHOORCAAV-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C=C(Cl)C(O)=C1
Synonyms:
  • Boronic acid, B-(2,4-dichloro-5-hydroxyphenyl)-
  • (2,4-Dichloro-5-hydroxyphenyl)boronic acid
  • B-(2,4-Dichloro-5-hydroxyphenyl)boronic acid
  • 2,4-Dichloro-5-hydroxyphenylboronic acid
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