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CAS 850568-34-2

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B-[3-(1-Piperidinylcarbonyl)phenyl]boronic acid

Description:
B-[3-(1-Piperidinylcarbonyl)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 piperidinylcarbonyl group, contributing to its potential biological activity and utility in medicinal chemistry. The piperidine moiety may enhance the compound's solubility and interaction with biological targets. Boronic acids are often utilized in various applications, including drug development, as they can participate in Suzuki coupling reactions, a key method in organic synthesis. Additionally, the presence of the boronic acid group allows for potential applications in sensing and as a therapeutic agent, particularly in the context of cancer research and treatment. The compound's structure suggests it may exhibit specific interactions with enzymes or receptors, making it a candidate for further investigation in pharmacological studies. Overall, B-[3-(1-Piperidinylcarbonyl)phenyl]boronic acid represents a versatile scaffold in the realm of organic and medicinal chemistry.
Formula:C12H16BNO3
InChI:InChI=1S/C12H16BNO3/c15-12(14-7-2-1-3-8-14)10-5-4-6-11(9-10)13(16)17/h4-6,9,16-17H,1-3,7-8H2
InChI key:InChIKey=XFTARKGZGNWJJT-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC(B(O)O)=CC=C1)N2CCCCC2
Synonyms:
  • 3-(Piperidin-1-ylcarbonyl)benzeneboronic acid
  • 3-(Piperidinocarbonyl)phenylboronic acid
  • B-[3-(1-Piperidinylcarbonyl)phenyl]boronic acid
  • Boronic acid, [3-(1-piperidinylcarbonyl)phenyl]-
  • [3-(Piperidin-1-ylcarbonyl)phenyl]boronic acid
  • [3-[(Piperidin-1-yl)carbonyl]phenyl]boronic acid
  • boronic acid, B-[3-(1-piperidinylcarbonyl)phenyl]-
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