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Atomfair 2-Methoxy-4-phenylaniline C13H13NO

Description 2-Methoxy-4-phenylaniline (CAS No. 39811-17-1) is a high-purity aromatic amine compound with the molecular formula C13H13NO . This fine chemical is characterized by its methoxy and phenyl substituents on an aniline backbone, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 199.25 g/mol, it is supplied as a crystalline solid with stringent quality control to ensure consistency for sensitive applications. Ideal for researchers in medicinal chemistry, material science, and dye synthesis, this compound is packaged under inert conditions to maintain stability. Available in quantities ranging from milligrams to kilograms, it is suited for…

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Description

Description

2-Methoxy-4-phenylaniline (CAS No. 39811-17-1) is a high-purity aromatic amine compound with the molecular formula C13H13NO. This fine chemical is characterized by its methoxy and phenyl substituents on an aniline backbone, making it a valuable intermediate in organic synthesis and pharmaceutical research. With a molecular weight of 199.25 g/mol, it is supplied as a crystalline solid with stringent quality control to ensure consistency for sensitive applications. Ideal for researchers in medicinal chemistry, material science, and dye synthesis, this compound is packaged under inert conditions to maintain stability. Available in quantities ranging from milligrams to kilograms, it is suited for both laboratory-scale experiments and industrial-scale production.

  • CAS No: 39811-17-1
  • Molecular Formula: C13H13NO
  • Molecular Weight: 199.25
  • Exact Mass: 199.099714038
  • Monoisotopic Mass: 199.099714038
  • IUPAC Name: 2-methoxy-4-phenylaniline
  • SMILES: COC1=C(C=CC(=C1)C2=CC=CC=C2)N
  • Synonyms: 2-methoxy-4-phenylaniline, 42271-43-2, 3-METHOXY-[1,1′-BIPHENYL]-4-AMINE, 3-Methoxy[1,1′-biphenyl]-4-amine, SCHEMBL358211

Application

2-Methoxy-4-phenylaniline serves as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and specialty dyes. Its aromatic amine functionality allows for further derivatization, making it useful in coupling reactions and heterocyclic compound formation. Researchers also employ it in the development of liquid crystal materials and organic electronic components due to its conjugated structure. Additionally, it may act as a precursor in the synthesis of bioactive molecules targeting neurological and inflammatory pathways.

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