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CAS 850567-30-5

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B-[3-[(4-Methyl-1-piperidinyl)carbonyl]phenyl]boronic acid

Description:
B-[3-[(4-Methyl-1-piperidinyl)carbonyl]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 and is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a piperidine moiety, which enhances its biological activity and solubility. The piperidine ring, containing a methyl group, contributes to the compound's lipophilicity and potential interactions with biological targets. Boronic acids are often utilized in the development of pharmaceuticals, particularly in the treatment of cancer and diabetes, due to their ability to inhibit specific enzymes. This compound's structure suggests it may have applications in drug discovery, particularly in the design of protease inhibitors or in the development of targeted therapies. Its unique characteristics, including its molecular geometry and functional groups, make it a valuable compound in both research and therapeutic contexts.
Formula:C13H18BNO3
InChI:InChI=1S/C13H18BNO3/c1-10-5-7-15(8-6-10)13(16)11-3-2-4-12(9-11)14(17)18/h2-4,9-10,17-18H,5-8H2,1H3
InChI key:InChIKey=KDLCYMDXPOEVCG-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC(B(O)O)=CC=C1)N2CCC(C)CC2
Synonyms:
  • B-[3-[(4-Methyl-1-piperidinyl)carbonyl]phenyl]boronic acid
  • Boronic acid, B-[3-[(4-methyl-1-piperidinyl)carbonyl]phenyl]-
  • Boronic acid, [3-[(4-methyl-1-piperidinyl)carbonyl]phenyl]-
  • Boronicacid, [3-[[(4-fluorophenyl)amino]carbonyl]phenyl]- (9CI)
  • [3-((4-Fluorophenyl)carbamoyl)phenyl]boronic acid
  • [3-(4-Methylpiperidine-1-carbonyl)phenyl]boronic acid
  • [3-[(4-Methylpiperidin-1-yl)carbonyl]phenyl]boronic acid
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