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CAS 182344-22-5

:

B-[4-[(2,2-Dimethyl-1-oxopropyl)amino]phenyl]boronic acid

Description:
B-[4-[(2,2-Dimethyl-1-oxopropyl)amino]phenyl]boronic acid, with the CAS number 182344-22-5, is a boronic acid derivative characterized by its unique functional groups that include a boron atom bonded to a phenyl ring and an amino group. 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 presence of the dimethyl-1-oxopropyl group enhances its solubility and reactivity. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. The compound may also exhibit biological activity, potentially serving as a pharmacophore in drug development. Its stability, reactivity, and ability to interact with biological molecules make it a subject of interest in both synthetic and medicinal chemistry. However, specific physical and chemical properties such as melting point, solubility, and spectral data would require empirical measurement or literature reference for precise characterization.
Formula:C11H16BNO3
InChI:InChI=1S/C11H16BNO3/c1-11(2,3)10(14)13-9-6-4-8(5-7-9)12(15)16/h4-7,15-16H,1-3H3,(H,13,14)
InChI key:InChIKey=ORNCMGDXLWQRHH-UHFFFAOYSA-N
SMILES:N(C(C(C)(C)C)=O)C1=CC=C(B(O)O)C=C1
Synonyms:
  • (4-(((tert-Butyl)carbonyl)amino)phenyl)boronic acid
  • (4-Pivalamidophenyl)boronic acid
  • 4-Pivalamidobenzeneboronic acid
  • 4-[(2,2-Dimethylpropanoyl)Amino]Benzeneboronic Acid
  • 4-[(2,2-Dimethylpropanoyl)amino]benzeneboronic acid 98%
  • B-[4-[(2,2-Dimethyl-1-oxopropyl)amino]phenyl]boronic acid
  • Boronic acid, B-[4-[(2,2-dimethyl-1-oxopropyl)amino]phenyl]-
  • Boronic acid, [4-[(2,2-dimethyl-1-oxopropyl)amino]phenyl]-
  • N-(4-Borono)phenylpivalamide
  • [4-(Pivaloylamino)phenyl]boronic acid
  • {4-[(2,2-Dimethylpropanoyl)Amino]Phenyl}Boronic Acid
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