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CAS 647853-32-5

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[3-(2-hydroxyethyl)phenyl]boronic acid

Description:
[3-(2-Hydroxyethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has a hydroxyethyl substituent. 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 presence of the hydroxyl group. 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 cross-coupling reactions. The boronic acid moiety allows for participation in Suzuki-Miyaura coupling reactions, which are essential in the formation of carbon-carbon bonds. Additionally, this compound may exhibit biological activity, particularly in the context of medicinal chemistry, where boronic acids are explored for their potential in drug development. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C8H11BO3
InChI:InChI=1/C8H11BO3/c10-5-4-7-2-1-3-8(6-7)9(11)12/h1-3,6,10-12H,4-5H2
SMILES:c1cc(CCO)cc(c1)B(O)O
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