2,9-Bis(naphthalen-2-YL)-4,7-diphenyl-1,10-phenanthroline

• CAT Number: L006633
• CAS Number: 1174006-43-9
• Molecular Formula: C44H28N2
• Molecular Weight: 584.70
• Purity: ≥95%
• Storage: Room Temperature (Recommended in a cool and dark place)
• IUPAC Name: 2,9-dinaphthalen-2-yl-4,7-diphenyl-1,10-phenanthroline
• InChI: InChI=1S/C44H28N2/c1-3-13-31(14-4-1)39-27-41(35-21-19-29-11-7-9-17-33(29)25-35)45-43-37(39)23-24-38-40(32-15-5-2-6-16-32)28-42(46-44(38)43)36-22-20-30-12-8-10-18-34(30)26-36/h1-28H
• InChIKey: XESMNQMWRSEIET-UHFFFAOYSA-N
• SMILES: C1=CC=C(C=C1)C2=CC(=NC3=C2C=CC4=C3N=C(C=C4C5=CC=CC=C5)C6=CC7=CC=CC=C7C=C6)C8=CC9=CC=CC=C9C=C8

2,9-Bis(naphthalen-2-yl)-4,7-diphenyl-1,10-phenanthroline(CAT: L006633) is a highly conjugated heteroaromatic compound widely applied in organic optoelectronics and coordination chemistry. Its extended π-system, combining phenanthroline, phenyl, and naphthyl substituents, delivers excellent electron-transport properties, strong photostability, and high thermal resistance. Frequently used in OLEDs, organic photovoltaic devices, and advanced electronic systems, this compound supports efficient charge balance and device performance. The phenanthroline core also functions as a versatile chelating ligand, forming stable metal complexes for applications in luminescent probes, catalysis, and photochemical research. Its dual functionality in materials science and coordination chemistry makes it an important tool for next-generation optoelectronic development.