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CAS 1218789-98-0

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2-(Aminocarbonylmethyl)phenylboronic acid, pinacol ester

Description:
2-(Aminocarbonylmethyl)phenylboronic acid, pinacol ester, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and an aminocarbonylmethyl substituent. 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 functionality enhances its stability and solubility, facilitating its use in reactions. The presence of the amino and carbonyl groups contributes to its reactivity, allowing it to participate in coupling reactions, particularly in the formation of carbon-carbon bonds. Additionally, the compound may exhibit moderate polarity due to the functional groups, influencing its solubility in different solvents. Overall, this compound is of interest in the development of pharmaceuticals and materials science, where boronic acids play a crucial role in drug design and synthesis methodologies.
Formula:C14H20BNO3
Synonyms:
  • 2-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
  • 2-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)
  • 2-(Aminocarbonylmethyl)phenylboronic acid, pinacol ester
  • 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzeneacetamide
  • Benzeneacetamide, 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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95
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100
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