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CAS 850568-16-0

:

B-[4-[[(2-Cyanoethyl)amino]carbonyl]phenyl]boronic acid

Description:
B-[4-[[(2-Cyanoethyl)amino]carbonyl]phenyl]boronic 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 and other nucleophiles. This compound features a phenyl ring substituted with a carbonyl group linked to a cyanoethylamino moiety, contributing to its potential reactivity and biological activity. The cyanoethyl group enhances the compound's solubility and may influence its interaction with biological targets. Boronic acids are often utilized in medicinal chemistry for their role in drug design, particularly in the development of proteasome inhibitors and in the synthesis of various organic compounds through Suzuki coupling reactions. The presence of the cyano group may also impart unique electronic properties, making this compound of interest in materials science and organic electronics. Overall, B-[4-[[(2-Cyanoethyl)amino]carbonyl]phenyl]boronic acid exhibits characteristics typical of boronic acids, including potential applications in pharmaceuticals and organic synthesis.
Formula:C10H11BN2O3
InChI:InChI=1S/C10H11BN2O3/c12-6-1-7-13-10(14)8-2-4-9(5-3-8)11(15)16/h2-5,15-16H,1,7H2,(H,13,14)
InChI key:InChIKey=QIZJQVHZGULPAE-UHFFFAOYSA-N
SMILES:C(NCCC#N)(=O)C1=CC=C(B(O)O)C=C1
Synonyms:
  • Boronic acid, [4-[[(2-cyanoethyl)amino]carbonyl]phenyl]-
  • Boronic acid, B-[4-[[(2-cyanoethyl)amino]carbonyl]phenyl]-
  • (4-((2-Cyanoethyl)carbamoyl)phenyl)boronic acid
  • (4-[[(2-Cyanoethyl)amino]carbonyl]phenyl)boronic acid
  • B-[4-[[(2-Cyanoethyl)amino]carbonyl]phenyl]boronic acid
  • 4-(2-CYANOETHYLAMINOCARBONYL)PHENYLBORONIC ACID
  • 4-(2-Cyanoethylaminocarbonyl)benzeneboronic acid ,96%
  • 4-(2-CYANOETHYLAMINOCARBONYL)BENZENEBORONIC ACID
  • 4-(2-Cyanoethylcarbamoyl)benzeneboronic acid, 96%
  • 4-(2-Cyanoethylaminocarbonyl)benzeneboronic acid 96%
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