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CAS 913835-26-4

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(3-amino-5-cyano-phenyl)boronic acid hydrochloride

Description:
(3-amino-5-cyano-phenyl)boronic acid hydrochloride is a boronic acid derivative characterized by the presence of an amino group and a cyano group on a phenyl ring, along with a boronic acid functional group. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and methanol, which is a common trait for many boronic acids. The presence of the amino group allows for potential interactions with biological systems, making it of interest in medicinal chemistry and drug development. The cyano group contributes to the compound's electronic properties, potentially enhancing its reactivity in various chemical reactions, including Suzuki coupling reactions, which are important in organic synthesis. As a hydrochloride salt, it is often more stable and easier to handle than its free base form. Overall, this compound is valuable in research and applications involving organic synthesis, pharmaceuticals, and materials science due to its unique functional groups and reactivity.
Formula:C7H8BClN2O2
InChI:InChI=1/C7H7BN2O2.ClH/c9-4-5-1-6(8(11)12)3-7(10)2-5;/h1-3,11-12H,10H2;1H
SMILES:c1c(cc(cc1B(O)O)N)C#N.Cl
Synonyms:
  • 3-Amino-5-cyanobenzeneboronic acid hydrochloride
  • B-(3-Amino-5-cyanophenyl)boronic acid, hydrochloride (1:1)
  • Qbqr Cz Ecn
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