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Atomfair N,N-Dimethyl-p-nitrosoaniline C8H10N2O

Description N,N-Dimethyl-p-nitrosoaniline (CAS No. 138-84-1) is a high-purity nitroso compound with the molecular formula C8H10N2O , widely utilized in organic synthesis and chemical research. This compound, also known by its IUPAC name N,N-dimethyl-4-nitrosoaniline , features a nitroso functional group attached to a dimethyl-substituted aniline ring, making it a valuable intermediate for the preparation of dyes, pharmaceuticals, and advanced materials. With its distinct green crystalline appearance, it is rigorously tested for purity and stability, ensuring optimal performance in sensitive applications. Suitable for laboratory and industrial use, this product is available in various quantities to meet your research needs. Store in a…

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Description

Description

N,N-Dimethyl-p-nitrosoaniline (CAS No. 138-84-1) is a high-purity nitroso compound with the molecular formula C8H10N2O, widely utilized in organic synthesis and chemical research. This compound, also known by its IUPAC name N,N-dimethyl-4-nitrosoaniline, features a nitroso functional group attached to a dimethyl-substituted aniline ring, making it a valuable intermediate for the preparation of dyes, pharmaceuticals, and advanced materials. With its distinct green crystalline appearance, it is rigorously tested for purity and stability, ensuring optimal performance in sensitive applications. Suitable for laboratory and industrial use, this product is available in various quantities to meet your research needs. Store in a cool, dry place away from light to maintain integrity.

  • CAS No: 138-84-1
  • Molecular Formula: C8H10N2O
  • Molecular Weight: 150.18
  • Exact Mass: 150.079312947
  • Monoisotopic Mass: 150.079312947
  • IUPAC Name: N,N-dimethyl-4-nitrosoaniline
  • SMILES: CN(C)C1=CC=C(C=C1)N=O
  • Synonyms: N,N-Dimethyl-4-nitrosoaniline, 138-89-6, Accelerine, p-Nitroso-N,N-dimethylaniline, 4-Nitrosodimethylaniline

Application

N,N-Dimethyl-p-nitrosoaniline is commonly employed as a reagent in organic synthesis, particularly in the preparation of azo dyes and other nitroso-derived compounds. It serves as a key intermediate in the development of photochromic materials and redox-active molecules for electrochemical studies. Researchers also utilize this compound in mechanistic studies of nitroso group reactivity due to its well-defined electronic properties.

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