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CAS 169760-16-1

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(2-Acetylaminophenyl)boronic acid

Description:
(2-Acetylaminophenyl)boronic acid is an organic compound characterized by the presence of both a boronic acid functional group and an acetylamino substituent on a phenyl ring. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The acetylamino group enhances its solubility in organic solvents and may influence its reactivity and biological activity. The compound is often utilized in the development of pharmaceuticals and as a building block in the synthesis of more complex molecules. Its structure allows for potential interactions with biological targets, which can be explored in drug design. Additionally, (2-Acetylaminophenyl)boronic acid may exhibit specific physical properties such as melting point and solubility, which are important for its practical applications. As with many boronic acids, it is essential to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C8H10BNO3
InChI:InChI=1/C8H10BNO3/c1-6(11)10-8-5-3-2-4-7(8)9(12)13/h2-5,12-13H,1H3,(H,10,11)
SMILES:CC(=Nc1ccccc1B(O)O)O
Synonyms:
  • 2-Acetamidophenylboronicacid
  • 2-Acetamidophenylboronic Acid
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