Description

2-(8-Bromodibenzo[b,d]furan-4-yl)-4,6-diphenyl-1,3,5-triazine (CAS No. 1821221-55-9) is a high-purity heterocyclic organic compound with the molecular formula C₂₇H₁₆BrN₃O. This advanced chemical features a dibenzofuran core functionalized with a bromine substituent at the 8-position and a diphenyl-1,3,5-triazine moiety at the 4-position, making it a valuable building block for materials science and pharmaceutical research. With a molecular weight of 478.35 g/mol, this compound exhibits excellent thermal and chemical stability, suitable for applications in OLEDs, optoelectronic materials, and as a ligand in catalytic systems. Available in quantities ranging from milligrams to bulk orders, our product is rigorously tested via HPLC, NMR, and mass spectrometry to ensure ≥95% purity. Store in a cool, dry environment away from light to maintain integrity.

Properties

• CAS Number: 1821221-55-9
• Complexity: 596
• IUPAC Name: 2-(8-bromodibenzofuran-4-yl)-4,6-diphenyl-1,3,5-triazine
• InChI: InChI=1S/C27H16BrN3O/c28-19-14-15-23-22(16-19)20-12-7-13-21(24(20)32-23)27-30-25(17-8-3-1-4-9-17)29-26(31-27)18-10-5-2-6-11-18/h1-16H
• InChI Key: RVZVSJCDYHXCFW-UHFFFAOYSA-N
• Exact Mass: 477.04767
• Molecular Formula: C27H16BrN3O
• Molecular Weight: 478.3
• SMILES: C1=CC=C(C=C1)C2=NC(=NC(=N2)C3=CC=CC4=C3OC5=C4C=C(C=C5)Br)C6=CC=CC=C6
• Topological: 51.8
• Monoisotopic Mass: 477.04767
• Synonyms: 1821221-55-9, 2-(8-Bromodibenzo[b,d]furan-4-yl)-4,6-diphenyl-1,3,5-triazine, SCHEMBL17225110, 2-{12-bromo-8-oxatricyclo[7.4.0.0?,?]trideca-1(13),2,4,6,9,11-hexaen-6-yl}-4,6-diphenyl-1,3,5-triazine

Application

This compound serves as a key intermediate in the synthesis of advanced organic semiconductors and light-emitting materials for OLED applications. Researchers utilize its rigid, planar structure to enhance charge transport properties in optoelectronic devices. Additionally, it finds use in coordination chemistry as a nitrogen-donor ligand for transition metal catalysts. Its bromine functionality allows for further derivatization via cross-coupling reactions in medicinal chemistry.

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