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CAS 871332-70-6

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B-[4-Chloro-3-(1-piperidinylcarbonyl)phenyl]boronic acid

Description:
B-[4-Chloro-3-(1-piperidinylcarbonyl)phenyl]boronic acid is an organoboron 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 chlorinated phenyl ring, which enhances its reactivity and potential biological activity. The piperidinylcarbonyl moiety introduces a nitrogen-containing heterocycle, contributing to its pharmacological properties. This compound is typically utilized in the development of pharmaceuticals, particularly in the synthesis of compounds targeting various biological pathways. Its boronic acid functionality allows for applications in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, the presence of the chlorine atom may influence the compound's lipophilicity and overall bioavailability. As with many boronic acids, it is important to handle this substance with care, considering its reactivity and potential environmental impact.
Formula:C12H15BClNO3
InChI:InChI=1S/C12H15BClNO3/c14-11-5-4-9(13(17)18)8-10(11)12(16)15-6-2-1-3-7-15/h4-5,8,17-18H,1-3,6-7H2
InChI key:InChIKey=QNOMMSMMADZNCM-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC(B(O)O)=CC=C1Cl)N2CCCCC2
Synonyms:
  • B-[4-Chloro-3-(1-piperidinylcarbonyl)phenyl]boronic acid
  • Boronic acid, [4-chloro-3-(1-piperidinylcarbonyl)phenyl]-
  • Boronicacid, [4-chloro-3-(1-piperidinylcarbonyl)phenyl]- (9CI)
  • [4-Chloro-3-(piperidine-1-carbonyl)phenyl]boronic acid
  • Boronic acid, B-[4-chloro-3-(1-piperidinylcarbonyl)phenyl]-
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