• 1. Emulsifier-free, organotellurium-mediated living radical emulsion polymerization (emulsion TERP) of styrene: poly(dimethylaminoethyl methacrylate) macro-TERP agent?
  Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
• 2. Fe3O4@PANI: a magnetic polyaniline nanomaterial for highly efficient and handy enrichment of intact N-glycopeptides??
  Zhizhen Lai,Mo Zhang,Jinyu Zhou,Tianjing Chen,Dan Li,Xuejing Shen,Jia Liu,Jiang Zhou,Zhili Li Analyst, 2021,146, 4261-4267
• 3. Exceptional activity of sub-nm Pt clusters on CdS for photocatalytic hydrogen production: a combined experimental and first-principles study?
  Qiyuan Wu,Shangmin Xiong,Peichuan Shen,Shen Zhao,Alexander Orlov Catal. Sci. Technol., 2015,5, 2059-2064
• 4. 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
• 5. Emergence of cationic polyamine dendrimersomes: design, stimuli sensitivity and potential biomedical applications
  Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026

4-Bromo-5-Ethoxy-N-Ethyl-2-Nitroaniline

The compound 4-Bromo-5-Ethoxy-N-Ethyl-2-Nitroaniline, with the CAS number 1280786-88-0, is a highly specialized organic chemical that has garnered significant attention in the fields of pharmaceutical research and materials science. This compound is characterized by its complex structure, which includes a bromine atom at the 4-position, an ethoxy group at the 5-position, and a nitro group at the 2-position on the aniline ring. The presence of these substituents imparts unique electronic and steric properties to the molecule, making it a valuable tool in various synthetic and analytical applications.

Recent studies have highlighted the potential of 4-Bromo-5-Ethoxy-N-Ethyl-2-Nitroaniline as a key intermediate in the synthesis of advanced materials, particularly in the development of novel polymers and high-performance composites. Researchers have demonstrated that this compound can serve as a building block for creating materials with enhanced mechanical strength and thermal stability, which are critical for applications in aerospace and automotive industries. The ability of this compound to undergo controlled polymerization reactions has been extensively explored in recent publications, underscoring its versatility in materials science.

In the pharmaceutical sector, 4-Bromo-5-Ethoxy-N-Ethyl-2-Nitroaniline has shown promise as a precursor for bioactive molecules. Its structure allows for selective substitution reactions, enabling the creation of derivatives with specific pharmacological properties. For instance, studies have revealed that certain derivatives of this compound exhibit potent anti-inflammatory and antioxidant activities, making them potential candidates for drug development. The nitro group at the 2-position plays a crucial role in these activities by influencing the molecule's redox properties and interactions with biological systems.

The synthesis of 4-Bromo-5-Ethoxy-N-Ethyl-2-Nitroaniline involves a multi-step process that typically begins with the nitration of an aniline derivative followed by bromination and ethoxylation. Recent advancements in catalytic methods have significantly improved the efficiency and selectivity of these reactions. For example, the use of palladium catalysts has been reported to enhance the yield and purity of the final product, reducing waste and environmental impact. These developments align with current trends toward sustainable chemical synthesis practices.

In terms of application, 4-Bromo-5-Ethoxy-N-Ethyl-2-Nitroaniline has also found utility in analytical chemistry as a chromophore in sensor devices. Its ability to undergo reversible redox reactions makes it suitable for use in electrochemical sensors designed to detect specific analytes in complex matrices. Recent research has focused on integrating this compound into wearable devices for real-time monitoring of environmental parameters, showcasing its potential in emerging technologies.

The structural uniqueness of 4-Bromo-5-Ethoxy-N-Ethyl-2-Nitroaniline also lends itself to applications in optoelectronics. Its conjugated system allows for strong absorption in the visible spectrum, making it a candidate for use in organic light-emitting diodes (OLEDs) and photovoltaic cells. Studies have demonstrated that derivatives of this compound can exhibit high quantum yields under specific conditions, contributing to advancements in energy-efficient lighting and renewable energy technologies.

In conclusion, 4-Bromo-5-Ethoxy-N-Ethyl-2-Nitroaniline, CAS No. 1280786-88-0, stands out as a versatile compound with diverse applications across multiple scientific disciplines. Its role as an intermediate in material synthesis, its potential in pharmaceutical development, and its contributions to optoelectronics highlight its significance in contemporary research. As ongoing studies continue to uncover new properties and applications, this compound is poised to play an increasingly important role in shaping future innovations across various industries.

• 1242336-59-9(4-Bromo-5-ethoxy-2-nitroaniline)
• 1311197-92-8(4-Bromo-N-methyl-2-nitro-5-propoxyaniline)
• 1280786-66-4(4-Bromo-N-(tert-butyl)-5-ethoxy-2-nitroaniline)
• 1280786-60-8(4-Bromo-N-ethyl-5-methoxy-2-nitroaniline)
• 1311197-83-7(4-Bromo-2-nitro-5-propoxy-N-propylaniline)
• 1280786-69-7(4-Bromo-5-methoxy-2-nitro-N-propylaniline)
• 62606-12-6(Benzenamine, N-(3-bromo-5-methoxyphenyl)-2,4,6-trinitro-)
• 1330750-43-0(4-Bromo-N-isopropyl-5-methoxy-2-nitroaniline)
• 7357-66-6(4-Acetamido-2-bromo-5-nitroanisole)
• 1280786-62-0(4-Bromo-5-ethoxy-2-nitro-N-propylaniline)