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CAS 397843-71-9

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B-[3-[(Phenylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-[(Phenylamino)carbonyl]phenyl]boronic acid, identified by its CAS number 397843-71-9, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a phenylamino and carbonyl group. 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 phenylamino group suggests potential interactions with biological targets, enhancing its relevance in drug discovery. Additionally, the boronic acid moiety can participate in Suzuki coupling reactions, a vital method for constructing carbon-carbon bonds in organic synthesis. The compound's solubility and stability can vary depending on the solvent and pH, which are critical factors to consider in its application. Overall, B-[3-[(Phenylamino)carbonyl]phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C13H12BNO3
InChI:InChI=1S/C13H12BNO3/c16-13(15-12-7-2-1-3-8-12)10-5-4-6-11(9-10)14(17)18/h1-9,17-18H,(H,15,16)
InChI key:InChIKey=ZFEJFNWZHUMGRH-UHFFFAOYSA-N
SMILES:C(NC1=CC=CC=C1)(=O)C2=CC(B(O)O)=CC=C2
Synonyms:
  • B-[3-[(Phenylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, [3-[(phenylamino)carbonyl]phenyl]-
  • [3-(Phenylcarbamoyl)phenyl]boronic acid
  • boronic acid, B-[3-[(phenylamino)carbonyl]phenyl]-
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