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CAS 762262-11-3

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{3-[(2-cyanoethyl)carbamoyl]phenyl}boronic acid

Description:
{3-[(2-cyanoethyl)carbamoyl]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 at the 3-position with a carbamoyl group linked to a cyanoethyl moiety, enhancing its reactivity and potential applications in organic synthesis and medicinal chemistry. The cyanoethyl group introduces a polar character, which can influence solubility and interaction with biological targets. Boronic acids are often utilized in Suzuki coupling reactions, making this compound valuable in the synthesis of complex organic molecules. Additionally, the presence of the cyano group may impart unique electronic properties, potentially affecting the compound's behavior in various chemical environments. Overall, {3-[(2-cyanoethyl)carbamoyl]phenyl}boronic acid is a versatile compound with applications in drug development and materials science, owing to its functional groups and reactivity profile.
Formula:C10H11BN2O3
InChI:InChI=1/C10H11BN2O3/c12-5-2-6-13-10(14)8-3-1-4-9(7-8)11(15)16/h1,3-4,7,15-16H,2,6H2,(H,13,14)
SMILES:c1cc(cc(c1)B(O)O)C(=NCCC#N)O
Synonyms:
  • 3-(2-Cyanoethylaminocarbonyl)phenylboronic acid
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