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Atomfair N-Benzylideneaniline C13H11N

Description N-Benzylideneaniline (CAS No. 538-51-2) is an organic compound with the molecular formula C13H11N and IUPAC name N,1-diphenylmethanimine . This Schiff base is characterized by its crystalline solid form and is widely utilized in organic synthesis, coordination chemistry, and material science research. Its structure features a benzylidene group (?CCH=) linked to an aniline moiety, making it a valuable intermediate for synthesizing heterocyclic compounds, ligands for metal complexes, and photochromic materials. High-purity N-Benzylideneaniline is essential for reproducible experimental results, and our product is rigorously tested for quality, ensuring optimal performance in research applications. Available in various quantities to suit laboratory-scale and…

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Description

Description

N-Benzylideneaniline (CAS No. 538-51-2) is an organic compound with the molecular formula C13H11N and IUPAC name N,1-diphenylmethanimine. This Schiff base is characterized by its crystalline solid form and is widely utilized in organic synthesis, coordination chemistry, and material science research. Its structure features a benzylidene group (?CCH=) linked to an aniline moiety, making it a valuable intermediate for synthesizing heterocyclic compounds, ligands for metal complexes, and photochromic materials. High-purity N-Benzylideneaniline is essential for reproducible experimental results, and our product is rigorously tested for quality, ensuring optimal performance in research applications. Available in various quantities to suit laboratory-scale and industrial needs.

  • CAS No: 538-51-2
  • Molecular Formula: C13H11N
  • Molecular Weight: 181.23
  • Exact Mass: 181.089149355
  • Monoisotopic Mass: 181.089149355
  • IUPAC Name: N,1-diphenylmethanimine
  • SMILES: C1=CC=C(C=C1)C=NC2=CC=CC=C2
  • Synonyms: N-Benzylideneaniline, 538-51-2, N-Benzalaniline, Benzylidene-phenyl-amine, NSC 736

Application

N-Benzylideneaniline is commonly employed as a key intermediate in organic synthesis, particularly in the preparation of Schiff base ligands for transition metal complexes. It serves as a precursor for photochromic and thermochromic materials due to its reversible isomerization properties. Researchers also utilize it in the development of liquid crystals and as a model compound for studying imine reactivity in catalytic systems.

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