tert-Butyl 2-(4-bromophenyl)-1H-pyrrole-1-carboxylate
97%
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This chemical is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring a bromophenyl group and a pyrrole ring, makes it valuable in the construction of pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the bromophenyl moiety into target molecules. Additionally, the tert-butyl carboxylate group serves as a protective group for the pyrrole nitrogen, enabling selective modifications during multi-step synthetic processes. Its applications extend to materials science, where it can be used to create functionalized polymers or organic electronic materials.
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