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Atomfair 4,6-dichloro-N,N-diphenyl-1,3,5-triazin-2-amine C15H10Cl2N4

Description 4,6-Dichloro-N,N-diphenyl-1,3,5-triazin-2-amine (CAS No. 16033-74-2) is a high-purity triazine derivative with the molecular formula C15H10Cl2N4. This compound features a 1,3,5-triazine core substituted with two chlorine atoms at the 4- and 6-positions and a diphenylamino group at the 2-position. It is a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and advanced materials. The compound is supplied as a fine crystalline powder with ??95% purity (HPLC), ensuring consistency for research and industrial applications. Store in a cool, dry place, protected from light and moisture to maintain stability.

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Description

Description

4,6-Dichloro-N,N-diphenyl-1,3,5-triazin-2-amine (CAS No. 16033-74-2) is a high-purity triazine derivative with the molecular formula C15H10Cl2N4. This compound features a 1,3,5-triazine core substituted with two chlorine atoms at the 4- and 6-positions and a diphenylamino group at the 2-position. It is a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and advanced materials. The compound is supplied as a fine crystalline powder with ??95% purity (HPLC), ensuring consistency for research and industrial applications. Store in a cool, dry place, protected from light and moisture to maintain stability.

  • CAS No: 16033-74-2
  • Molecular Formula: C15H10Cl2N4
  • Molecular Weight: 317.2
  • Exact Mass: 316.0282517
  • Monoisotopic Mass: 316.0282517
  • IUPAC Name: 4,6-dichloro-N,N-diphenyl-1,3,5-triazin-2-amine
  • SMILES: C1=CC=C(C=C1)N(C2=CC=CC=C2)C3=NC(=NC(=N3)Cl)Cl
  • Synonyms: 4,6-dichloro-N,N-diphenyl-1,3,5-triazin-2-amine, 16033-74-2, DTXSID50274830, DTXCID20226285, Oprea1_707211

Application

4,6-Dichloro-N,N-diphenyl-1,3,5-triazin-2-amine is widely used as a key intermediate in the synthesis of heterocyclic compounds, including potential pharmaceutical candidates and agrochemicals. Its reactive chlorine sites enable nucleophilic substitution reactions, making it valuable for constructing complex triazine-based scaffolds. Researchers also explore its utility in materials science, such as photoactive polymers or coordination chemistry.

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