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CAS 957034-87-6

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[2-(1-piperidylsulfonyl)phenyl]boronic acid

Description:
[2-(1-Piperidylsulfonyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and organic synthesis. The compound features a phenyl ring substituted with a piperidylsulfonyl group, contributing to its unique chemical properties. The piperidine moiety enhances the compound's solubility and reactivity, while the sulfonyl group can participate in various chemical reactions, including nucleophilic substitutions. This compound is typically used in the development of pharmaceuticals, particularly in the synthesis of biologically active molecules. Its boronic acid functionality allows it to act as a key intermediate in cross-coupling reactions, such as Suzuki coupling, which is widely utilized in the formation of carbon-carbon bonds. Overall, [2-(1-piperidylsulfonyl)phenyl]boronic acid is a versatile compound with significant implications in both research and industrial applications.
Formula:C11H16BNO4S
InChI:InChI=1/C11H16BNO4S/c14-12(15)10-6-2-3-7-11(10)18(16,17)13-8-4-1-5-9-13/h2-3,6-7,14-15H,1,4-5,8-9H2
SMILES:C1CCN(CC1)S(=O)(=O)c1ccccc1B(O)O
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