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CAS 486422-58-6

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[4-(1-piperidylsulfonyl)phenyl]boronic acid

Description:
[4-(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. This compound features a phenyl ring substituted with a piperidylsulfonyl group, contributing to its unique chemical properties. The piperidine ring enhances its solubility and reactivity, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. The sulfonyl group can also impart additional polar characteristics, influencing the compound's interactions in biological systems. This compound is often utilized in medicinal chemistry and materials science due to its potential applications in drug development and as a building block in the synthesis of complex organic molecules. Its boronic acid functionality allows it to participate in the formation of boronate esters, which are important in the development of sensors and in the study of biomolecular interactions.
Formula:C11H16BNO4S
InChI:InChI=1/C11H16BNO4S/c14-12(15)10-4-6-11(7-5-10)18(16,17)13-8-2-1-3-9-13/h4-7,14-15H,1-3,8-9H2
SMILES:C1CCN(CC1)S(=O)(=O)c1ccc(cc1)B(O)O
Synonyms:
  • [4-(Piperidin-1-Ylsulfonyl)Phenyl]Boronic Acid
  • boronic acid, B-[4-(1-piperidinylsulfonyl)phenyl]-
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