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CAS 874288-26-3

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B-[3-[[[(3-Chlorophenyl)methyl]amino]carbonyl]phenyl]boronic acid

Description:
B-[3-[[[(3-Chlorophenyl)methyl]amino]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. This compound features a chlorophenyl moiety, contributing to its potential biological activity and interactions. The presence of the amino and carbonyl groups suggests that it may participate in various chemical reactions, including those involving nucleophilic attack or hydrogen bonding. Boronic acids are often utilized in medicinal chemistry for their role in drug design, particularly in the development of protease inhibitors and in the synthesis of complex organic molecules through Suzuki coupling reactions. The specific structure of this compound may also influence its solubility, stability, and reactivity, making it of interest in both research and pharmaceutical applications. As with many boronic acids, it may exhibit pH-dependent behavior, affecting its ionization state and reactivity in different environments.
Formula:C14H13BClNO3
InChI:InChI=1S/C14H13BClNO3/c16-13-6-1-3-10(7-13)9-17-14(18)11-4-2-5-12(8-11)15(19)20/h1-8,19-20H,9H2,(H,17,18)
InChI key:InChIKey=YCYWAZBKGRQQNH-UHFFFAOYSA-N
SMILES:C(NCC1=CC(Cl)=CC=C1)(=O)C2=CC(B(O)O)=CC=C2
Synonyms:
  • Boronic acid, B-[3-[[[(3-chlorophenyl)methyl]amino]carbonyl]phenyl]-
  • Boronic acid, [3-[[[(3-chlorophenyl)methyl]amino]carbonyl]phenyl]-
  • B-[3-[[[(3-Chlorophenyl)methyl]amino]carbonyl]phenyl]boronic acid
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