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CAS 957120-47-7

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B-[3-Chloro-5-(1-piperidinylcarbonyl)phenyl]boronic acid

Description:
B-[3-Chloro-5-(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, making it useful in various chemical applications, including organic synthesis and medicinal chemistry. The compound features a chlorinated phenyl ring and a piperidinylcarbonyl substituent, which contribute to its biological activity and potential as a pharmaceutical intermediate. The boronic acid moiety allows for participation in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds. This compound is typically solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its reactivity and functional groups make it a valuable building block in the synthesis of complex organic molecules. Safety data should be consulted for handling, as boronic acids can pose health risks if not managed properly. Overall, this compound exemplifies the versatility of boron-containing compounds in synthetic organic chemistry.
Formula:C12H15BClNO3
InChI:InChI=1S/C12H15BClNO3/c14-11-7-9(6-10(8-11)13(17)18)12(16)15-4-2-1-3-5-15/h6-8,17-18H,1-5H2
InChI key:InChIKey=YDTRQMGRXMDOJG-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC(B(O)O)=CC(Cl)=C1)N2CCCCC2
Synonyms:
  • 3-Chloro-5-(piperidine-1-carbonyl)phenylboronic acid
  • B-[3-Chloro-5-(1-piperidinylcarbonyl)phenyl]boronic acid
  • Boronic acid, B-[3-chloro-5-(1-piperidinylcarbonyl)phenyl]-
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