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  Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
• 2. An Assessment of the Laminar Hypersonic Double-Cone Experiments in the LENS-XX Tunnel
  JaideepRay,PatrickBlonigan,EricT.Phipps,KathrynMaupin
• 3. An algal process treatment combined with the Fenton reaction for high concentrations of amoxicillin and cefradine
  Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Quinolines and derivatives Phenylquinolines

5-Phenyl-1,10-phenanthroline (CAS No. 6153-89-5): A Versatile Compound for Advanced Applications

5-Phenyl-1,10-phenanthroline (CAS No. 6153-89-5) is a highly specialized organic compound that has garnered significant attention in both academic and industrial research. This heterocyclic compound, belonging to the phenanthroline family, is known for its unique structural properties and wide-ranging applications. The presence of a phenyl group at the 5-position of the 1,10-phenanthroline backbone enhances its electronic and steric characteristics, making it a valuable building block in various chemical syntheses.

The compound's molecular formula is C₁₈H₁₂N₂, and it exhibits a molecular weight of 256.30 g/mol. Its crystalline structure and solubility in organic solvents like dichloromethane and dimethyl sulfoxide (DMSO) make it suitable for diverse applications. Researchers often utilize 5-Phenyl-1,10-phenanthroline as a ligand in coordination chemistry due to its ability to form stable complexes with transition metals. This property is particularly relevant in the development of luminescent materials and catalysts, which are currently hot topics in materials science.

One of the most exciting applications of 5-Phenyl-1,10-phenanthroline is in the field of organic electronics. With the growing demand for flexible displays and light-emitting diodes (OLEDs), this compound has emerged as a key component in the synthesis of high-performance emissive layers. Its ability to facilitate electron transport and enhance device efficiency has made it a subject of intense research. Recent studies have also explored its potential in solar cells, where it acts as an electron-transporting material, contributing to improved photovoltaic performance.

In addition to its electronic applications, 5-Phenyl-1,10-phenanthroline plays a crucial role in supramolecular chemistry. Its rigid aromatic structure and nitrogen donor atoms enable the formation of well-defined molecular assemblies. This has led to its use in the design of molecular sensors and drug delivery systems, addressing current challenges in healthcare and environmental monitoring. The compound's compatibility with biomolecules further expands its utility in bioconjugation and diagnostic imaging.

The synthesis of 5-Phenyl-1,10-phenanthroline typically involves the Skraup reaction or Pictet-Spengler cyclization, followed by functionalization at the 5-position. Researchers are continually optimizing these methods to improve yield and purity, catering to the increasing demand for high-quality material. The compound's stability under ambient conditions and its compatibility with standard laboratory protocols make it a preferred choice for both academic and industrial settings.

Market trends indicate a rising interest in 5-Phenyl-1,10-phenanthroline, driven by advancements in optoelectronics and nanotechnology. Companies specializing in fine chemicals and advanced materials are investing in scalable production methods to meet the needs of research institutions and manufacturers. The compound's versatility ensures its relevance in emerging fields such as quantum computing and artificial intelligence (AI)-enabled materials, aligning with global technological trends.

For researchers and industry professionals seeking reliable sources of 5-Phenyl-1,10-phenanthroline, it is essential to partner with reputable suppliers who adhere to stringent quality control measures. The compound's purity, typically verified by high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy, is critical for achieving consistent results in experimental and commercial applications.

In summary, 5-Phenyl-1,10-phenanthroline (CAS No. 6153-89-5) is a multifaceted compound with significant potential in cutting-edge technologies. Its applications span organic electronics, supramolecular chemistry, and advanced materials, making it a valuable asset for researchers and innovators. As scientific exploration continues to evolve, this compound is poised to play an even greater role in shaping the future of technology and industry.

• 91237-66-0(Ruthenium(2+),tris(4,7-diphenyl-1,10-phenanthroline-kN1,kN10)-, (OC-6-11-L)- (9CI))
• 94552-81-5(Rhodium(3+),tris(4,7-diphenyl-1,10-phenanthroline-kN1,kN10)-, (OC-6-11)-)
• 1215007-80-9(4,7-Di(naphthalen-1-yl)-1,10-phenanthroline)
• 89460-94-6(Tris(diphenylphenanthroline)cobalt(III))
• 96761-79-4(biphens)
• 1662-01-7(Bathophenanthroline)
• 62366-01-2(1,10-Phenanthroline,4-phenyl-)
• 36309-88-3(Tris(4,7-diphenyl-1,10-phenanthroline)ruthenium(II) dichloride)
• 68309-97-7(tris(4,7-diphenyl-1,10-phenanthroline-N1,N10)nickel(2+) bis[tetrafluoroborate(1-)])
• 96710-07-5(4,7-Di([1,1'-biphenyl]-4-yl)-1,10-phenanthroline)