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Atomfair N-(2-(p-bromophenoxy)ethyl)pyrrolidine C12H16BrNO

Description N-(2-(p-bromophenoxy)ethyl)pyrrolidine (CAS No. 1081-73-8) is a high-purity organic compound with the molecular formula C12H16BrNO . This specialized chemical features a pyrrolidine moiety linked to a 4-bromophenoxyethyl group, making it a valuable intermediate in pharmaceutical and agrochemical research. Its IUPAC name, 1-[2-(4-bromophenoxy)ethyl]pyrrolidine , reflects its precise molecular structure. This compound is supplied as a crystalline solid or solution, with rigorous QC testing to ensure >98% purity (HPLC). Ideal for use in Suzuki couplings, nucleophilic substitutions, and as a ligand precursor. Packaged under inert gas in amber glass vials to ensure stability. SDS and analytical data (GC/MS, NMR) available upon request.

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Description

Description

N-(2-(p-bromophenoxy)ethyl)pyrrolidine (CAS No. 1081-73-8) is a high-purity organic compound with the molecular formula C12H16BrNO. This specialized chemical features a pyrrolidine moiety linked to a 4-bromophenoxyethyl group, making it a valuable intermediate in pharmaceutical and agrochemical research. Its IUPAC name, 1-[2-(4-bromophenoxy)ethyl]pyrrolidine, reflects its precise molecular structure. This compound is supplied as a crystalline solid or solution, with rigorous QC testing to ensure >98% purity (HPLC). Ideal for use in Suzuki couplings, nucleophilic substitutions, and as a ligand precursor. Packaged under inert gas in amber glass vials to ensure stability. SDS and analytical data (GC/MS, NMR) available upon request.

  • CAS No: 1081-73-8
  • Molecular Formula: C12H16BrNO
  • Molecular Weight: 270.17
  • Exact Mass: 269.04153
  • Monoisotopic Mass: 269.04153
  • IUPAC Name: 1-[2-(4-bromophenoxy)ethyl]pyrrolidine
  • SMILES: C1CCN(C1)CCOC2=CC=C(C=C2)Br
  • Synonyms: 1081-73-8, 1-(2-(4-bromophenoxy)ethyl)pyrrolidine, 1-[2-(4-Bromophenoxy)ethyl]pyrrolidine, N-(2-(p-Bromophenoxy)ethyl)pyrrolidine, EINECS 214-100-9

Application

N-(2-(p-bromophenoxy)ethyl)pyrrolidine serves as a key building block in medicinal chemistry for developing dopamine receptor ligands. Researchers utilize this compound in palladium-catalyzed cross-coupling reactions to create novel heterocyclic systems. Its bromophenoxy group makes it particularly useful in structure-activity relationship (SAR) studies for CNS-targeting pharmaceuticals. The compound has shown utility in the synthesis of potential antipsychotic agents through reductive amination pathways.

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