Description

2-Chloro-4-dibenzofuran-4-yl-6-phenyl-[1,3,5]triazine (CAS No. 1472729-25-1) is a high-purity heterocyclic compound with the molecular formula C₂₁H₁₂ClN₃O. This specialized organic chemical features a triazine core substituted with a chloro group, a phenyl ring, and a dibenzofuran moiety, making it a valuable intermediate for advanced synthetic applications. Its well-defined structure and high reactivity enable precise modifications in pharmaceutical, agrochemical, and materials science research. Suitable for use in cross-coupling reactions, ligand synthesis, and as a building block for optoelectronic materials, this compound is rigorously tested for purity and consistency. Packaged under inert conditions to ensure stability, it is ideal for researchers requiring reliable and high-performance reagents.

Properties

• CAS Number: 1472729-25-1
• Complexity: 486
• IUPAC Name: 2-chloro-4-dibenzofuran-4-yl-6-phenyl-1,3,5-triazine
• InChI: InChI=1S/C21H12ClN3O/c22-21-24-19(13-7-2-1-3-8-13)23-20(25-21)16-11-6-10-15-14-9-4-5-12-17(14)26-18(15)16/h1-12H
• InChI Key: NKLKYZYRMGGYGN-UHFFFAOYSA-N
• Exact Mass: 357.0668897
• Molecular Formula: C21H12ClN3O
• Molecular Weight: 357.8
• SMILES: C1=CC=C(C=C1)C2=NC(=NC(=N2)Cl)C3=CC=CC4=C3OC5=CC=CC=C45
• Topological: 51.8
• Monoisotopic Mass: 357.0668897
• Synonyms: 1472729-25-1, 2-Chloro-4-dibenzofuran-4-yl-6-phenyl-[1,3,5]triazine, 2-Chloro-4-(dibenzo[b,d]furan-4-yl)-6-phenyl-1,3,5-triazine, SCHEMBL16636998, 2-Chloro-4-(4-dibenzofuranyl)-6-phenyl-1,3,5-triazine, MFCD32215036, BS-48632, DB-192552, F71504, 2-chloro-4-dibenzofuran-4-yl-6-phenyl-1,3,5-triazine, 2-Chloro-4-dibenzofuran-4-yl-6-phenyl[1,3,5]triazine

Application

2-Chloro-4-dibenzofuran-4-yl-6-phenyl-[1,3,5]triazine is primarily utilized as a key intermediate in the synthesis of advanced organic materials, including optoelectronic compounds and pharmaceutical agents. Its triazine scaffold and dibenzofuran substitution make it suitable for designing ligands in catalytic systems or as a core structure in fluorescent dyes. Researchers also employ this compound in cross-coupling reactions to develop novel polymers or small molecules with tailored electronic properties. Its versatility supports applications in organic light-emitting diodes (OLEDs) and other high-tech material sciences.

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