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CAS 146140-95-6

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2-(tert-Butylcarbonylamino)phenylboronic acid

Description:
2-(tert-Butylcarbonylamino)phenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a tert-butylcarbonylamino group. This compound typically exhibits properties associated with both boronic acids and amines, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and materials science. The tert-butylcarbonyl group enhances the stability and solubility of the compound, while the boronic acid moiety can participate in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. Additionally, the compound may exhibit moderate acidity due to the boronic acid group, which can influence its reactivity and interactions in biological systems. Overall, 2-(tert-Butylcarbonylamino)phenylboronic acid is a versatile compound with potential applications in drug development and synthetic organic chemistry.
Formula:C11H16BNO3
InChI:InChI=1/C11H16BNO3/c1-11(2,3)10(14)13-9-7-5-4-6-8(9)12(15)16/h4-7,15-16H,1-3H3,(H,13,14)
SMILES:CC(C)(C)C(=Nc1ccccc1B(O)O)O
Synonyms:
  • 2-(Pivaloylamino)phenylboronic acid
  • 2-[(2,2-Dimethylpropanoyl)amino]phenylboronic acid
  • 2-(2,2-Dimethyl-Propionylamino)phenylboronic acid
  • Akos Brn-0489
  • 2-(Pivaloylamino)benzeneboronic acid
  • 2-(2,2,2-Trimethylacetamido)benzeneboronic acid
  • {2-[(2,2-Dimethylpropanoyl)Amino]Phenyl}Boronic Acid
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