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Atomfair 4-Aminodiphenyl ether C12H11NO

Description 4-Aminodiphenyl ether (CAS 139-59-3) , also known as 4-phenoxyaniline , is a high-purity aromatic amine compound with the molecular formula C12H11NO . This fine chemical is widely utilized in organic synthesis, pharmaceutical intermediates, and advanced material research. Its structure features an amino group (-NH2) para-substituted to a phenoxy moiety, making it a valuable building block for heterocyclic compounds and functional polymers. Available in crystalline powder form with ??98% purity (HPLC), it is rigorously tested for consistency, low heavy metal content, and minimal impurities. Suitable for use under inert conditions due to potential air sensitivity. Packaged in amber glass bottles…

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Description

Description

4-Aminodiphenyl ether (CAS 139-59-3), also known as 4-phenoxyaniline, is a high-purity aromatic amine compound with the molecular formula C12H11NO. This fine chemical is widely utilized in organic synthesis, pharmaceutical intermediates, and advanced material research. Its structure features an amino group (-NH2) para-substituted to a phenoxy moiety, making it a valuable building block for heterocyclic compounds and functional polymers. Available in crystalline powder form with ??98% purity (HPLC), it is rigorously tested for consistency, low heavy metal content, and minimal impurities. Suitable for use under inert conditions due to potential air sensitivity. Packaged in amber glass bottles or vacuum-sealed bags to ensure stability and longevity.

  • CAS No: 139-59-3
  • Molecular Formula: C12H11NO
  • Molecular Weight: 185.22
  • Exact Mass: 185.084063974
  • Monoisotopic Mass: 185.084063974
  • IUPAC Name: 4-phenoxyaniline
  • SMILES: C1=CC=C(C=C1)OC2=CC=C(C=C2)N
  • Synonyms: 4-PHENOXYANILINE, 139-59-3, 4-Aminodiphenyl ether, p-Phenoxyaniline, 4-Phenoxybenzenamine

Application

4-Aminodiphenyl ether serves as a key intermediate in the synthesis of dyes, agrochemicals, and liquid crystal materials. Researchers employ it in Suzuki coupling reactions to construct biaryl systems for pharmaceutical development. Its electron-rich aromatic structure also makes it useful in polymer chemistry for creating thermally stable resins and conductive materials.

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