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Atomfair Benzenamine, 3-(methylthio)-N-phenyl- C13H13NS

Description 3-Methylsulfanyl-N-phenylaniline (CAS No. 13313-45-6) is a high-purity organic compound with the molecular formula C13H13NS . This aromatic amine derivative features a methylthio (-SMe) substituent at the 3-position of the aniline ring, making it a valuable intermediate in synthetic organic chemistry and materials science. With a molecular weight of 215.31 g/mol, it is a yellow to light brown crystalline solid under standard conditions. Its unique structure enables applications in pharmaceuticals, agrochemicals, and specialty polymers. This product is rigorously tested for purity (typically ??95% by GC/HPLC) and is supplied with comprehensive analytical data, including1H NMR and FT-IR spectra. Suitable for research…

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Description

Description

3-Methylsulfanyl-N-phenylaniline (CAS No. 13313-45-6) is a high-purity organic compound with the molecular formula C13H13NS. This aromatic amine derivative features a methylthio (-SMe) substituent at the 3-position of the aniline ring, making it a valuable intermediate in synthetic organic chemistry and materials science. With a molecular weight of 215.31 g/mol, it is a yellow to light brown crystalline solid under standard conditions. Its unique structure enables applications in pharmaceuticals, agrochemicals, and specialty polymers. This product is rigorously tested for purity (typically ??95% by GC/HPLC) and is supplied with comprehensive analytical data, including 1H NMR and FT-IR spectra. Suitable for research and industrial use, it is packaged under inert gas to ensure stability.

  • CAS No: 13313-45-6
  • Molecular Formula: C13H13NS
  • Molecular Weight: 215.32
  • Exact Mass: 215.07687059
  • Monoisotopic Mass: 215.07687059
  • IUPAC Name: 3-methylsulfanyl-N-phenylaniline
  • SMILES: CSC1=CC=CC(=C1)NC2=CC=CC=C2
  • Synonyms: Benzenamine, 3-(methylthio)-N-phenyl-, EINECS 236-342-4, 3-(Methylthio)-N-phenylaniline, 13313-45-6, 3-methylsulfanyl-N-phenylaniline

Application

3-Methylsulfanyl-N-phenylaniline serves as a key building block in the synthesis of heterocyclic compounds and functionalized anilines. It is utilized in pharmaceutical research for developing bioactive molecules, particularly those targeting CNS disorders. The compound’s electron-rich aromatic system makes it suitable for metal-catalyzed cross-coupling reactions in materials science. Additionally, it finds use in agrochemical formulations as a precursor for sulfur-containing pesticides.

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