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CAS 850568-23-9

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B-[4-[(4-Oxo-1-piperidinyl)carbonyl]phenyl]boronic acid

Description:
B-[4-[(4-Oxo-1-piperidinyl)carbonyl]phenyl]boronic acid, with the CAS number 850568-23-9, is a boronic acid derivative characterized by its boron atom bonded to a phenyl group and a piperidinyl moiety. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and organic synthesis. The presence of the piperidinyl group suggests potential biological activity, as piperidine derivatives are often found in pharmaceuticals. The carbonyl functionality enhances the compound's reactivity and may influence its interaction with biological targets. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. Overall, this compound's unique structure and functional groups contribute to its potential utility in drug development and synthetic chemistry.
Formula:C12H14BNO4
InChI:InChI=1S/C12H14BNO4/c15-11-5-7-14(8-6-11)12(16)9-1-3-10(4-2-9)13(17)18/h1-4,17-18H,5-8H2
InChI key:InChIKey=AIAPQNNEMPKYKZ-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC=C(B(O)O)C=C1)N2CCC(=O)CC2
Synonyms:
  • Boronic acid, [4-[(4-oxo-1-piperidinyl)carbonyl]phenyl]-
  • B-[4-[(4-Oxo-1-piperidinyl)carbonyl]phenyl]boronic acid
  • Boronic acid, B-[4-[(4-oxo-1-piperidinyl)carbonyl]phenyl]-
  • [4-(4-Oxopiperidine-1-carbonyl)phenyl]boronic acid
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