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CAS 947533-21-3

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(6-acetamido-3-pyridyl)boronic acid

Description:
(6-acetamido-3-pyridyl)boronic acid is an organic compound characterized by the presence of a pyridine ring substituted with an acetamido group and a boronic acid functional group. The molecular structure features a boron atom bonded to a hydroxyl group and an aromatic ring, which contributes to its reactivity and potential applications in medicinal chemistry and materials science. This compound typically exhibits moderate solubility in polar solvents due to the presence of the boronic acid moiety, which can form reversible covalent bonds with diols, making it useful in various chemical reactions, including Suzuki coupling reactions. The acetamido group enhances the compound's stability and solubility, while also potentially influencing its biological activity. As a boronic acid derivative, it may have applications in drug development, particularly in the design of inhibitors for certain enzymes or in the synthesis of complex organic molecules. Overall, (6-acetamido-3-pyridyl)boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C7H9BN2O3
InChI:InChI=1/C7H9BN2O3/c1-5(11)10-7-3-2-6(4-9-7)8(12)13/h2-4,12-13H,1H3,(H,9,10,11)
SMILES:CC(=Nc1ccc(cn1)B(O)O)O
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