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CAS 1310384-34-9

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Boronic acid, B-(5-amino-3-pyridinyl)-, hydrochloride (1:1)

Description:
Boronic acid, B-(5-amino-3-pyridinyl)-, hydrochloride (1:1) is a chemical compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that contains an amino substituent. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to its ionic nature when in hydrochloride form. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including organic synthesis and medicinal chemistry. The presence of the amino group enhances its reactivity and potential for biological activity, which may be relevant in drug development. Additionally, the hydrochloride form indicates that the compound is a salt, which can influence its stability and solubility properties. Overall, this compound is of interest in both academic research and pharmaceutical applications due to its unique structural features and reactivity.
Formula:C5H7BN2O2·ClH
InChI:InChI=1S/C5H7BN2O2.ClH/c7-5-1-4(6(9)10)2-8-3-5;/h1-3,9-10H,7H2;1H
InChI key:InChIKey=FFNXDGUUZKYZGR-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C(N)C=NC1.Cl
Synonyms:
  • (5-Aminopyridin-3-yl)boronic acid hydrochloride
  • Boronic acid, B-(5-amino-3-pyridinyl)-, hydrochloride (1:1)
  • 5-AMinopyridine-3-boronic acidHCl
  • boronic acid hydrochloride
  • (5-Aminopyridin-3-yl)
  • (5-amino-3-pyridyl)boronic acid
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