Description

2-(4-Bromonaphthalen-1-yl)-4,6-diphenyl-1,3,5-triazine (CAS No. 1800228-86-7) is a high-purity organic compound with the molecular formula C₂₅H₁₆BrN₃. This specialized triazine derivative features a bromonaphthalene moiety coupled with two phenyl groups, making it a valuable intermediate for advanced organic synthesis and materials science research. With a molecular weight of 438.32 g/mol, this compound is ideal for applications in photoluminescent materials, organic electronics, and as a building block for supramolecular chemistry. Our product is rigorously tested for purity and stability, ensuring reliable performance in sensitive experimental conditions. Available in research quantities with detailed technical data, this compound is a must-have for chemists and material scientists exploring novel aromatic systems.

Properties

• CAS Number: 1800228-86-7
• Complexity: 490
• IUPAC Name: 2-(4-bromo-1-naphthyl)-4,6-diphenyl-1,3,5-triazine
• InChI: InChI=1S/C25H16BrN3/c26-22-16-15-21(19-13-7-8-14-20(19)22)25-28-23(17-9-3-1-4-10-17)27-24(29-25)18-11-5-2-6-12-18/h1-16H
• InChI Key: JLGXRQBMJFAZRY-UHFFFAOYSA-N
• Exact Mass: 437.05276
• Molecular Formula: C25H16BrN3
• Molecular Weight: 438.3
• SMILES: C1=CC=C(C=C1)C2=NC(=NC(=N2)C3=CC=C(C4=CC=CC=C43)Br)C5=CC=CC=C5
• Topological: 38.7
• Monoisotopic Mass: 437.05276
• Synonyms: 1800228-86-7, 2-(4-bromonaphthalen-1-yl)-4,6-diphenyl-1,3,5-triazine, 1,3,5-Triazine, 2-(4-bromo-1-naphthalenyl)-4,6-diphenyl-, 2-(4-Bromo-1-naphthalenyl)-4,6-diphenyl-1,3,5-triazine, MFCD30469069, SCHEMBL18347061, BS-51830, SY283441, DB-103607, CS-0186412, E77118, 2-(4-Bromo-1-naphthyl)-4,6-diphenyl-1,3,5-triazine

Application

2-(4-Bromonaphthalen-1-yl)-4,6-diphenyl-1,3,5-triazine is primarily used as a key intermediate in the synthesis of advanced organic materials, particularly in the development of luminescent compounds and optoelectronic devices. Its unique structure makes it suitable for research in organic light-emitting diodes (OLEDs) and photovoltaic applications. Additionally, this compound serves as a versatile scaffold in supramolecular chemistry for designing novel aromatic frameworks. Researchers also utilize it in cross-coupling reactions to create complex polycyclic systems with tailored electronic properties.

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