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CAS 380430-61-5

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(2-Acetylaminophenyl)boronic acid, pinacol ester

Description:
(2-Acetylaminophenyl)boronic acid, pinacol ester, is an organoboron compound characterized by the presence of a boronic acid moiety and an acetylamino group attached to 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 pinacol ester formation enhances its stability and solubility in organic solvents. The presence of the acetylamino group can influence its reactivity and interactions, potentially allowing for selective binding in biological systems. This compound may also participate in Suzuki-Miyaura cross-coupling reactions, which are vital in the synthesis of complex organic molecules. Overall, (2-Acetylaminophenyl)boronic acid, pinacol ester is a versatile building block in the development of pharmaceuticals and agrochemicals, contributing to the advancement of materials science and chemical biology.
Formula:C14H20BNO3
InChI:InChI=1/C14H20BNO3/c1-10(17)16-12-9-7-6-8-11(12)15-18-13(2,3)14(4,5)19-15/h6-9H,1-5H3,(H,16,17)
SMILES:CC(=Nc1ccccc1B1OC(C)(C)C(C)(C)O1)O
Synonyms:
  • N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetamide
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