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CAS 625470-96-4

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3-[(Benzylamino)carbonyl]phenylboronic acid

Description:
3-[(Benzylamino)carbonyl]phenylboronic 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. This compound features a phenyl ring substituted with a benzylamino group and a carbonyl moiety, contributing to its potential reactivity and biological activity. The boronic acid group allows for participation in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis and medicinal chemistry. The presence of the benzylamino group may enhance solubility and facilitate interactions with biological targets, making this compound of interest in drug development and material science. Additionally, the compound's structure suggests potential applications in sensor technology and catalysis due to the unique properties of boron. Overall, 3-[(Benzylamino)carbonyl]phenylboronic acid exemplifies the versatility of boronic acids in synthetic and medicinal chemistry.
Formula:C14H14BNO3
InChI:InChI=1/C14H14BNO3/c17-14(16-10-11-5-2-1-3-6-11)12-7-4-8-13(9-12)15(18)19/h1-9,18-19H,10H2,(H,16,17)
SMILES:c1ccc(cc1)CN=C(c1cccc(c1)B(O)O)O
Synonyms:
  • [3-(Benzylcarbamoyl)phenyl]boronic acid
  • boronic acid, B-[3-[[(phenylmethyl)amino]carbonyl]phenyl]-
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