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CAS 874288-02-5

:

B-[4-[[(4-Chlorophenyl)amino]carbonyl]phenyl]boronic acid

Description:
B-[4-[[(4-Chlorophenyl)amino]carbonyl]phenyl]boronic acid, identified by its CAS number 874288-02-5, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an amino carbonyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the 4-chlorophenyl group enhances its biological activity and solubility in organic solvents. Additionally, the compound may exhibit moderate to high stability under standard laboratory conditions, although it can be sensitive to moisture and air. Its structural features suggest potential applications in drug development, particularly in the design of inhibitors for certain enzymes or receptors. Overall, this compound represents a valuable tool in both synthetic and pharmaceutical chemistry due to its unique reactivity and functional properties.
Formula:C13H11BClNO3
InChI:InChI=1S/C13H11BClNO3/c15-11-5-7-12(8-6-11)16-13(17)9-1-3-10(4-2-9)14(18)19/h1-8,18-19H,(H,16,17)
InChI key:InChIKey=KQGSKPWDDNXYNQ-UHFFFAOYSA-N
SMILES:C(NC1=CC=C(Cl)C=C1)(=O)C2=CC=C(B(O)O)C=C2
Synonyms:
  • 4-(4-Chlorophenylcarbamoyl)phenylboronic acid
  • B-[4-[[(4-Chlorophenyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, B-[4-[[(4-chlorophenyl)amino]carbonyl]phenyl]-
  • Boronic acid, [4-[[(4-chlorophenyl)amino]carbonyl]phenyl]-
  • [4-[(4-Chlorophenyl)carbamoyl]phenyl]boronic acid
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