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CAS 1451392-96-3

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B-[2-Chloro-4-(1-piperidinylcarbonyl)phenyl]boronic acid

Description:
B-[2-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 play a crucial role in Suzuki coupling reactions. This compound features a chlorinated phenyl ring and a piperidinylcarbonyl substituent, contributing to its potential biological activity and utility in medicinal chemistry. The boronic acid moiety allows for interactions with biological targets, making it of interest in drug development, particularly in the context of cancer therapeutics and other diseases. The presence of the piperidine ring may enhance its lipophilicity and facilitate cellular uptake. Additionally, the compound's structural features suggest it may exhibit specific reactivity patterns, making it valuable in synthetic organic chemistry. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C12H15BClNO3
InChI:InChI=1S/C12H15BClNO3/c14-11-8-9(4-5-10(11)13(17)18)12(16)15-6-2-1-3-7-15/h4-5,8,17-18H,1-3,6-7H2
InChI key:InChIKey=JWZDVWRFPJMCCV-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC(Cl)=C(B(O)O)C=C1)N2CCCCC2
Synonyms:
  • B-[2-Chloro-4-(1-piperidinylcarbonyl)phenyl]boronic acid
  • [2-Chloro-4-(piperidine-1-carbonyl)phenyl]boronic acid
  • Boronic acid, B-[2-chloro-4-(1-piperidinylcarbonyl)phenyl]-
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