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CAS 397843-80-0

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{4-[(phenylcarbonyl)amino]phenyl}boronic acid

Description:
{4-[(Phenylcarbonyl)amino]phenyl}boronic acid, with the CAS number 397843-80-0, is an organic compound that features a boronic acid functional group, which is characterized by the presence of a boron atom bonded to a hydroxyl group and an organic substituent. This compound contains an aromatic system, specifically a phenyl group, which contributes to its stability and reactivity. The presence of the phenylcarbonylamino group indicates that it has both amine and carbonyl functionalities, which can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Boronic acids are known for their ability to form reversible complexes with diols, making them useful in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Additionally, this compound may exhibit properties such as solubility in polar solvents and potential applications in materials science and catalysis. Its specific reactivity and applications would depend on the context of its use in chemical reactions or as a building block in more complex molecular architectures.
Formula:C13H12BNO3
InChI:InChI=1/C13H12BNO3/c16-13(10-4-2-1-3-5-10)15-12-8-6-11(7-9-12)14(17)18/h1-9,17-18H,(H,15,16)
SMILES:c1ccc(cc1)C(=O)Nc1ccc(cc1)B(O)O
Synonyms:
  • [4-(Benzoylamino)phenyl]boronic acid
  • boronic acid, B-[4-(benzoylamino)phenyl]-
  • (4-Benzamidophenyl)boronic acid
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