• 1. An inter-tangled network of redox-active and conducting polymers as a cathode for ultrafast rechargeable batteries
  Jieun Kim,Han-Saem Park,Tae-Hee Kim,Sung Yeol Kim,Hyun-Kon Song Phys. Chem. Chem. Phys., 2014,16, 5295-5300
• 2. Ambient electrochemical NH3 synthesis from N2 and water enabled by ZrO2 nanoparticles?
  Tong Xu,Dongwei Ma,Chengbo Li,Qian Liu,Siyu Lu,Abdullah M. Asiri,Chun Yang,Xuping Sun Chem. Commun., 2020,56, 3673-3676
• 3. Achieving molecular stability of racemic 4-O-benzyl-myo-inositol-1,3,5-orthoformate through crystal formation?
  Richa Sardessai,Shobhana Krishnaswamy,Mysore S. Shashidhar CrystEngComm, 2012,14, 8010-8016
• 4. An autoreduction method to prepare plasmonic gold-embedded polypeptide micelles for synergistic chemo-photothermal therapy?
  Xingjie Wu,Linzhu Zhou,Yue Su,Chang-Ming Dong J. Mater. Chem. B, 2016,4, 2142-2152
• 5. An ionic liquid-based synergistic extraction strategy for rare earths?
  Yingbo Li,Nada Mehio,Huizhou Liu,Sheng Dai Green Chem., 2015,17, 2981-2993

Comprehensive Overview of 1,4-Benzenediamine, N1,N4-bis(4-bromophenyl)-N1,N4-diphenyl- (CAS No. 525602-17-9)

The compound 1,4-Benzenediamine, N1,N4-bis(4-bromophenyl)-N1,N4-diphenyl- (CAS No. 525602-17-9) is a specialized aromatic amine derivative with significant applications in advanced material science and organic synthesis. This molecule features a central 1,4-benzenediamine core substituted with 4-bromophenyl and phenyl groups, making it a valuable intermediate in the development of high-performance polymers, liquid crystals, and optoelectronic materials. Its unique structural properties have garnered attention in both academic research and industrial applications.

One of the key reasons for the growing interest in 1,4-Benzenediamine, N1,N4-bis(4-bromophenyl)-N1,N4-diphenyl- is its role in the synthesis of advanced organic semiconductors. With the rise of flexible electronics and wearable technology, researchers are increasingly exploring novel materials that offer superior charge transport properties. This compound, with its extended π-conjugation and bromine substituents, serves as a precursor for designing high-efficiency OLEDs and organic photovoltaic cells. Recent studies highlight its potential in improving device performance, aligning with the global push for sustainable energy solutions.

In addition to its electronic applications, 1,4-Benzenediamine, N1,N4-bis(4-bromophenyl)-N1,N4-diphenyl- is also investigated for its use in liquid crystal displays (LCDs). The bromine atoms enhance molecular polarizability, which is critical for tuning the mesomorphic properties of liquid crystals. As the demand for high-resolution displays grows—driven by trends in augmented reality (AR) and virtual reality (VR)—this compound’s ability to stabilize liquid crystal phases makes it a candidate for next-generation display technologies.

The synthesis of 1,4-Benzenediamine, N1,N4-bis(4-bromophenyl)-N1,N4-diphenyl- typically involves palladium-catalyzed cross-coupling reactions, such as the Buchwald-Hartwig amination, to attach the aromatic substituents. Researchers are optimizing these protocols to improve yield and scalability, addressing the need for cost-effective production methods in industrial settings. Environmental considerations are also shaping synthetic strategies, with greener solvents and catalysts being explored to reduce the ecological footprint of chemical manufacturing.

From a commercial perspective, the market for 1,4-Benzenediamine derivatives is expanding, particularly in Asia-Pacific regions where electronics manufacturing is concentrated. Suppliers of 525602-17-9 are focusing on high-purity grades to meet the stringent requirements of optoelectronic applications. Pricing trends reflect the compound’s niche status, with premiums for research-grade quantities. Industry reports suggest that partnerships between academic institutions and material science firms are accelerating the adoption of this compound in cutting-edge technologies.

Safety and handling of 1,4-Benzenediamine, N1,N4-bis(4-bromophenyl)-N1,N4-diphenyl- follow standard laboratory protocols for aromatic amines. While not classified as hazardous under most regulatory frameworks, proper ventilation and personal protective equipment (PPE) are recommended during handling. Storage conditions typically involve protection from light and moisture to maintain stability, as brominated compounds can be sensitive to degradation under prolonged exposure to environmental factors.

Looking ahead, the versatility of CAS No. 525602-17-9 positions it as a molecule of interest for interdisciplinary research. Innovations in supramolecular chemistry and nanotechnology may unlock further applications, such as molecular sensors or catalytic frameworks. As sustainability becomes a priority, bio-based routes for synthesizing such compounds could emerge, aligning with circular economy principles. For researchers and manufacturers alike, staying updated on patent filings and academic publications related to this compound is essential to capitalize on its potential.

In summary, 1,4-Benzenediamine, N1,N4-bis(4-bromophenyl)-N1,N4-diphenyl- represents a convergence of chemistry, materials science, and engineering. Its role in enabling next-generation technologies underscores the importance of continued investment in specialized chemical research. For those seeking detailed technical data or procurement options, consulting reputable chemical databases and suppliers with certifications like ISO 9001 is advised to ensure quality and compliance.

• 93-46-9(ASM-DNT)
• 86-56-6(N,N-Dimethyl-1-naphthylamine)
• 90-30-2(N-Phenyl-1-napthyl Amine)
• 74-31-7(N1,N4-Diphenylbenzene-1,4-diamine)
• 99-97-8(4-Dimethylamino Toluene)
• 91-66-7(N,N-Diethylaniline)
• 93-05-0(N,N-Diethyl-P-phenylenediamine)
• 100-22-1(N,N,N',N'-Tetramethyl-p-phenylenediamine)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)