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CAS 874219-18-8

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B-[4-Methoxy-3-(1-piperidinylsulfonyl)phenyl]boronic acid

Description:
B-[4-Methoxy-3-(1-piperidinylsulfonyl)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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a methoxy group and a piperidinylsulfonyl moiety, which contribute to its solubility and reactivity. It is typically a white to off-white solid and is soluble in polar organic solvents. The presence of the piperidine ring suggests potential biological activity, as piperidine derivatives are often found in pharmaceuticals. This compound is primarily utilized in medicinal chemistry and research applications, particularly in the development of targeted therapies and as a building block in organic synthesis. Its boronic acid functionality also allows for the formation of complexes with biomolecules, which can be leveraged in drug design and delivery systems. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C12H18BNO5S
InChI:InChI=1S/C12H18BNO5S/c1-19-11-6-5-10(13(15)16)9-12(11)20(17,18)14-7-3-2-4-8-14/h5-6,9,15-16H,2-4,7-8H2,1H3
InChI key:InChIKey=DRXNMNKYEDFECK-UHFFFAOYSA-N
SMILES:S(=O)(=O)(C1=C(OC)C=CC(B(O)O)=C1)N2CCCCC2
Synonyms:
  • Boronic acid, [4-methoxy-3-(1-piperidinylsulfonyl)phenyl]-
  • B-[4-Methoxy-3-(1-piperidinylsulfonyl)phenyl]boronic acid
  • Boronic acid, B-[4-methoxy-3-(1-piperidinylsulfonyl)phenyl]-
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