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.

Properties

• CAS Number: 16033-74-2
• Complexity: 291
• IUPAC Name: 4,6-dichloro-N,N-diphenyl-1,3,5-triazin-2-amine
• InChI: InChI=1S/C15H10Cl2N4/c16-13-18-14(17)20-15(19-13)21(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
• InChI Key: UIKAQTBBQJSDQE-UHFFFAOYSA-N
• Exact Mass: 316.0282517
• Molecular Formula: C15H10Cl2N4
• Molecular Weight: 317.2
• SMILES: C1=CC=C(C=C1)N(C2=CC=CC=C2)C3=NC(=NC(=N3)Cl)Cl
• Topological: 41.9
• Monoisotopic Mass: 316.0282517
• Synonyms: 4,6-dichloro-N,N-diphenyl-1,3,5-triazin-2-amine, 16033-74-2, DTXSID50274830, DTXCID20226285, Oprea1_707211, Oprea1_836376, MLS000561367, (4,6-Dichloro-[1,3,5]triazin-2-yl)-diphenyl-amine, SCHEMBL6633842, CHEMBL1428205, UIKAQTBBQJSDQE-UHFFFAOYSA-N, HMS2519M19, STL194008, AKOS000593881, 2-diphenylamino-4,6-dichloro-s-triazine, NCGC00245038-01, CL-28786, SMR000174064, WS-02633, 2,4-dichloro-6-diphenylamino-sym-triazine, D86728, N-(2,4-Dichlor-1,3,5-triazino)-N-phenylanilin

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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