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CAS 115377-94-1

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1,1-Dimethylethyl N-(2-boronophenyl)carbamate

Description:
1,1-Dimethylethyl N-(2-boronophenyl)carbamate, with the CAS number 115377-94-1, is an organic compound characterized by its unique structure, which includes a carbamate functional group and a boron-containing aromatic moiety. This compound typically exhibits properties associated with both the carbamate and boron functionalities, such as potential reactivity in nucleophilic substitution reactions and the ability to form coordination complexes due to the presence of boron. It may be utilized in various applications, including organic synthesis and as a potential intermediate in the development of pharmaceuticals or agrochemicals. The presence of the dimethyl group contributes to steric hindrance, which can influence its reactivity and interaction with other molecules. Additionally, the compound's solubility, stability, and reactivity can vary depending on the solvent and environmental conditions. As with many boron-containing compounds, it may also exhibit interesting electronic properties, making it a subject of interest in materials science and medicinal chemistry. Safety and handling precautions should be observed due to potential toxicity associated with carbamate derivatives.
Formula:C11H16BNO4
InChI:InChI=1S/C11H16BNO4/c1-11(2,3)17-10(14)13-9-7-5-4-6-8(9)12(15)16/h4-7,15-16H,1-3H3,(H,13,14)
InChI key:InChIKey=RMEIKYSECODAHJ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(NC(OC(C)(C)C)=O)C=CC=C1
Synonyms:
  • (2-BOC-aminophenyl)boronic acid
  • 1,1-Dimethylethyl N-(2-boronophenyl)carbamate
  • Carbamic acid, (2-boronophenyl)-, C-(1,1-dimethylethyl) ester
  • Carbamic acid, N-(2-boronophenyl)-, 1,1-dimethylethyl ester
  • N-(tert-Butoxycarbonyl)-2-amino-1-phenylboronic acid
  • {2-[(Tert-Butoxycarbonyl)Amino]Phenyl}Boronic Acid
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