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CAS 943321-89-9

:

tert-butyl N-(5-bromothiophen-2-yl)carbamate

Description:
Tert-butyl N-(5-bromothiophen-2-yl)carbamate is an organic compound characterized by its carbamate functional group, which is derived from the reaction of an amine with a carbonic acid derivative. This compound features a tert-butyl group, providing steric hindrance and influencing its solubility and reactivity. The presence of the 5-bromothiophen-2-yl moiety introduces a bromine atom, which can enhance the compound's reactivity in nucleophilic substitution reactions and may also affect its electronic properties. The thiophene ring contributes to the compound's aromatic character, potentially influencing its stability and interactions with other molecules. Tert-butyl N-(5-bromothiophen-2-yl)carbamate may be utilized in various applications, including medicinal chemistry and material science, due to its unique structural features. Its properties, such as melting point, boiling point, and solubility, would depend on the specific conditions and the presence of other functional groups. As with many organic compounds, safety and handling precautions should be observed, particularly due to the presence of bromine, which can be hazardous.
Formula:C9H12BrNO2S
Synonyms:
  • 1,1-Dimethylethyl (5-Bromo-2-Thienyl)Carbamate
  • (5-Bromothiophen-2-Yl)-Carbamic Acid Tertbutyl Ester
  • tert-Butyl (5-bromothiophen-2-yl)carbamate
  • Rw2772
  • AmbkkkkK520
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