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CAS 850589-50-3

:

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

Description:
B-[3-Chloro-4-(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 for biological activity. The piperidinylcarbonyl substituent contributes to its lipophilicity and may influence its interaction with biological targets. This compound is typically utilized in the development of pharmaceuticals, particularly in the synthesis of protease inhibitors and other therapeutic agents. Its boronic acid moiety allows for participation in Suzuki coupling reactions, making it valuable in the construction of complex organic molecules. Additionally, the presence of the chlorine atom may affect its electronic properties and solubility. Overall, B-[3-Chloro-4-(1-piperidinylcarbonyl)phenyl]boronic acid is a versatile compound with significant implications in chemical research and drug development.
Formula:C12H15BClNO3
InChI:InChI=1S/C12H15BClNO3/c14-11-8-9(13(17)18)4-5-10(11)12(16)15-6-2-1-3-7-15/h4-5,8,17-18H,1-3,6-7H2
InChI key:InChIKey=AQTGPCIHLDJZJF-UHFFFAOYSA-N
SMILES:C(=O)(C1=C(Cl)C=C(B(O)O)C=C1)N2CCCCC2
Synonyms:
  • [3-Chloro-4-(piperidine-1-carbonyl)phenyl]boronic acid
  • Boronic acid, B-[3-chloro-4-(1-piperidinylcarbonyl)phenyl]-
  • B-[3-Chloro-4-(1-piperidinylcarbonyl)phenyl]boronic acid
  • Boronic acid, [3-chloro-4-(1-piperidinylcarbonyl)phenyl]-
  • [3-Chloro-4-(piperidin-1-ylcarbonyl)phenyl]boronic acid
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