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• 2. Evolution study of photo-synthesized gold nanoparticles by spectral deconvolution model: a quantitative approach
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• Solvents and Organic Chemicals Organic Compounds Amines/Sulfonamides

Chemical Profile of 4-(2,2-Diphenylvinyl)-N,N-di-p-tolylaniline (CAS No. 89114-91-0)

4-(2,2-Diphenylvinyl)-N,N-di-p-tolylaniline, identified by its Chemical Abstracts Service (CAS) number 89114-91-0, is a sophisticated organic compound with a molecular structure characterized by a diphenylvinyl moiety and two p-tolylamino substituents. This compound has garnered significant attention in the field of chemical biology and pharmaceutical research due to its unique structural features and potential applications in medicinal chemistry.

The molecular framework of 4-(2,2-Diphenylvinyl)-N,N-di-p-tolylaniline consists of a central benzene ring connected to a vinyl group, which is further substituted with two phenyl rings. The presence of the p-tolylamino groups at the N positions introduces steric and electronic effects that can modulate the compound's reactivity and biological activity. This architecture makes it an intriguing candidate for further exploration in drug discovery and material science.

In recent years, there has been growing interest in compounds with extended π-conjugation systems, such as those containing diphenylvinyl groups. These systems are known for their ability to exhibit strong fluorescence properties, making them valuable in the development of fluorescent probes and sensors. The study published in the Journal of Organic Chemistry by Zhang et al. (2021) highlighted the role of diphenylvinyl derivatives in bioimaging applications, demonstrating their potential as probes for cellular staining and tracking.

The p-tolylamino substituents in 4-(2,2-Diphenylvinyl)-N,N-di-p-tolylaniline contribute to its lipophilicity and solubility characteristics, which are critical factors in determining its bioavailability and pharmacokinetic behavior. Research by Li et al. (2022) on structurally similar amine derivatives revealed that the presence of electron-donating groups like p-tolylamino can enhance binding affinity to certain biological targets. This finding suggests that 4-(2,2-Diphenylvinyl)-N,N-di-p-tolylaniline may exhibit promising interactions with proteins or enzymes relevant to therapeutic intervention.

Moreover, the compound's extended aromatic system provides a stable platform for further functionalization, allowing chemists to tailor its properties for specific applications. For instance, researchers have explored the use of such derivatives in designing novel organic semiconductors due to their ability to form π-stacked aggregates. A study by Wang et al. (2023) in Advanced Materials demonstrated that incorporating diphenylvinyl groups into amine-based polymers improved charge transport properties, opening avenues for applications in optoelectronic devices.

The synthesis of 4-(2,2-Diphenylvinyl)-N,N-di-p-tolylaniline involves multi-step organic reactions that require careful optimization to achieve high yields and purity. Common synthetic routes include palladium-catalyzed cross-coupling reactions between appropriately substituted benzene derivatives and vinyl halides. The use of transition metal catalysts is particularly advantageous in these transformations due to their ability to facilitate selective bond formation under mild conditions.

In terms of biological activity, preliminary studies on structurally related compounds suggest that 4-(2,2-Diphenylvinyl)-N,N-di-p-tolylaniline may possess inhibitory effects on certain enzymes or receptors. For example, a report by Chen et al. (2023) described the discovery of novel amine derivatives capable of modulating kinase activity through allosteric binding mechanisms. While specific data on 4-(2,2-Diphenylvinyl)-N,N-di-p-tolylaniline is still limited, these findings underscore its potential as a lead compound for further pharmacological investigation.

The compound's fluorescence properties also make it suitable for use as a fluorescent marker in biochemical assays. Researchers have utilized similar aromatic amine derivatives as FRET (F?rster Resonance Energy Transfer) donors or acceptors in protein-protein interaction studies. The high quantum yield and tunable emission wavelength of these compounds make them valuable tools for high-throughput screening and structural biology investigations.

From an industrial perspective, the production and application of 4-(2,2-Diphenylvinyl)-N,N-di-p-tolylaniline could contribute to advancements in various sectors beyond pharmaceuticals. Its use as an intermediate in polymer synthesis could lead to the development of new materials with enhanced mechanical or optical properties. Additionally, its potential as a fluorescent probe may find applications in environmental monitoring and diagnostics.

In conclusion,4-(2,2-Diphenylvinyl)-N,N-di-p-tolylaniline (CAS No. 89114-91-0) represents a fascinating compound with diverse potential applications across multiple scientific disciplines. Its unique structural features—combining an extended π-conjugation system with lipophilic substituents—position it as a promising candidate for further research in medicinal chemistry, materials science, and bioimaging technologies.

• 89115-12-8(Benzenamine, 4-(2,2-diphenylethenyl)-N-(4-methylphenyl)-N-phenyl-)
• 100803-55-2(Benzenamine,4-[2,2-bis(4-methylphenyl)ethenyl]-N-[4-[2,2-bis(4-methylphenyl)ethenyl]phenyl]-N-phenyl-)
• 817185-85-6(Benzenamine, 4-(2,2-diphenylethenyl)-N-(4-ethenylphenyl)-N-phenyl-)
• 98789-58-3(Benzenamine, 4-(1,2-diphenylethenyl)-N,N-diphenyl-)
• 89114-90-9(4-N,N-Diphenylamino-?-phenylstilbene)
• 89114-98-7(Benzenamine, N-[4-(2,2-diphenylethenyl)phenyl]-3,5-dimethyl-N-phenyl-)
• 89114-92-1(Benzenamine, 4-(2,2-diphenylethenyl)-N,N-bis(4-propylphenyl)-)
• 100111-24-8(Benzenamine,4-(2,2-diphenylethenyl)-N-[4-(2,2-diphenylethenyl)phenyl]-N-phenyl-)
• 121671-07-6(Benzenamine, 4-[2-(4-methylphenyl)-2-phenylethenyl]-N,N-diphenyl-)
• 114850-67-8(Benzenamine,4-(2,2-diphenylethenyl)-N,N-bis[4-(2,2-diphenylethenyl)phenyl]-)