• 1. Evolved polymerases facilitate selection of fully 2′-OMe-modified aptamers?
  Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
• 2. Fe3O4/PEG-SO3H as a heterogeneous and magnetically-recyclable nanocatalyst for the oxidation of sulfides to sulfones or sulfoxides
  Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
• 3. Elusive 2-aminofuran Diels–Alder substrates for a straightforward synthesis of polysubstituted anilines?
  Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
• 4. Excitable dynamics in the bromate–sulfite–ferrocyanide reaction
  J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
• 5. Evolution of calcium phosphate precipitation in hanging drop vapor diffusion by in situRaman microspectroscopy
  Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Azoles Phenyl-1,3-oxazoles
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Azoles Oxazoles Phenyl-1,3-oxazoles

Comprehensive Overview of 4,5-Diphenyl-oxazol-2-ylamine (CAS No. 33119-63-0): Properties, Applications, and Research Insights

4,5-Diphenyl-oxazol-2-ylamine (CAS No. 33119-63-0) is a specialized organic compound belonging to the oxazole family, characterized by its unique molecular structure featuring two phenyl groups attached to an oxazole ring. This compound has garnered significant attention in pharmaceutical and materials science research due to its versatile chemical properties and potential applications. The CAS number 33119-63-0 serves as a critical identifier for researchers and industry professionals seeking precise information about this compound.

In recent years, the demand for 4,5-Diphenyl-oxazol-2-ylamine has increased, particularly in the development of novel fluorescent probes and organic electronic materials. Its structural rigidity and electron-rich nature make it an excellent candidate for optoelectronic applications, a topic frequently searched by users interested in advanced material science. Researchers often inquire about its synthesis methods, solubility, and thermal stability, reflecting the compound's relevance in cutting-edge technologies.

The compound's pharmaceutical potential is another area of growing interest. Studies suggest that derivatives of 4,5-Diphenyl-oxazol-2-ylamine may exhibit bioactive properties, sparking investigations into their use as enzyme inhibitors or therapeutic agents. This aligns with trending searches related to drug discovery and medicinal chemistry, where users seek information on small molecule therapeutics and their mechanisms of action.

From a synthetic chemistry perspective, the preparation of CAS No. 33119-63-0 typically involves cyclization reactions of appropriately substituted precursors. Optimization of these methods to improve yield and purity remains a key focus for chemists, as evidenced by frequent queries about scalable synthesis protocols. The compound's crystallographic data and spectroscopic characteristics (including NMR and mass spectrometry profiles) are also commonly requested by analytical laboratories.

Environmental and green chemistry considerations have become increasingly important in discussions about 4,5-Diphenyl-oxazol-2-ylamine. Researchers are exploring eco-friendly synthesis routes and biodegradability aspects of such compounds, reflecting broader societal concerns about chemical sustainability. These topics frequently appear in academic searches alongside terms like green solvents and catalyst design.

In material science applications, the compound's photophysical properties make it valuable for developing organic light-emitting diodes (OLEDs) and sensors. Its ability to exhibit aggregation-induced emission (AIE) has been particularly noteworthy, connecting to popular searches about luminescent materials and smart coatings. The structure-property relationships of such derivatives are actively studied to enhance performance in these applications.

Quality control and analytical characterization of 4,5-Diphenyl-oxazol-2-ylamine are essential for its reliable use across industries. Common analytical challenges include ensuring isomeric purity and detecting trace impurities, topics that generate substantial discussion in quality assurance forums. The compound's HPLC methods and storage stability are additional technical aspects frequently queried by laboratory professionals.

Looking forward, research directions for CAS No. 33119-63-0 are expanding into nanotechnology and hybrid material development. Its potential incorporation into molecular machines or supramolecular assemblies represents an exciting frontier, aligning with searches about next-generation functional materials. The compound's versatility ensures its continued relevance across multiple scientific disciplines.

• 77151-48-5(bis(4-Methoxyphenyl)-1,3-oxazol-2-amine)
• 20503-85-9(1,3-Propanediamine,N3-(4,5-diphenyl-2-oxazolyl)-N1,N1-dimethyl-)
• 20503-75-7(Oxazole, 4,5-diphenyl-2-((2-hydroxyethyl)amino)-)
• 4675-18-7(4,5-Diphenyloxazole)
• 89705-81-7(2-Oxazolamine, 4,5-diphenyl-N-2-propynyl-)
• 6116-92-3(2(3H)-Oxazolone, 4,5-diphenyl-, hydrazone)
• 14070-15-6(2-Oxazolamine,N,N-dimethyl-4,5-diphenyl-)
• 33119-67-4(5-ethyl-4-phenyl-1,3-oxazol-2-amine)
• 20503-83-7(2-((2-(Dimethylamino)ethyl)amino)-4,5-diphenyloxazole)
• 20503-68-8(2-(Butylamino)-4,5-diphenyloxazole)