• 1. Exciplex emission from the mixed dimer of naphthalene and 2-cyanonaphthalene in a supersonic jet
  Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
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  Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
• 3. Excellent energy storage performance in NaNbO3-based relaxor antiferroeic ceramics under a low electric field
  XuxinCheng,XiaomingChen,PengyuanFan
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  Min Kim,Jae-Joon Lee,Tengling Ye,Panagiotis E. Keivanidis,Kilwon Cho J. Mater. Chem. C, 2020,8, 1686-1696
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Anilides Aromatic anilides

N-(3-FORMYLPHENYL)-4-METHOXYBENZAMIDE: A Comprehensive Overview

N-(3-FORMYLPHENYL)-4-METHOXYBENZAMIDE, identified by the CAS number 885459-73-4, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound is characterized by its unique structure, which combines a benzamide moiety with a 3-formylphenyl group. The benzamide core is a common structural element in many biologically active compounds, making N-(3-FORMYLPHENYL)-4-METHOXYBENZAMIDE a promising candidate for various applications in drug discovery and material science.

Recent studies have highlighted the potential of N-(3-FORMYLPHENYL)-4-METHOXYBENZAMIDE in the development of novel therapeutic agents. Researchers have focused on its ability to modulate key biological pathways, such as those involved in inflammation and oxidative stress. For instance, a 2023 study published in the *Journal of Medicinal Chemistry* demonstrated that this compound exhibits potent anti-inflammatory activity by inhibiting the production of pro-inflammatory cytokines. This finding underscores its potential as a lead compound for the treatment of inflammatory diseases such as arthritis and cardiovascular disorders.

In addition to its pharmacological applications, N-(3-FORMYLPHENYL)-4-METHOXYBENZAMIDE has also been explored for its role in materials science. The compound's ability to form stable crystalline structures has led to its investigation as a component in advanced polymer materials. A 2022 study in *Materials Today* reported that incorporating this compound into polymer matrices significantly enhances their thermal stability and mechanical properties. This opens up new possibilities for its use in high-performance materials for aerospace and electronics industries.

The synthesis of N-(3-FORMYLPHENYL)-4-METHOXYBENZAMIDE involves a multi-step process that combines traditional organic synthesis techniques with modern catalytic methods. The key steps include the preparation of the benzamide derivative and the subsequent coupling with the 3-formylphenyl group. Researchers have optimized these steps to achieve high yields and purity, ensuring the compound's suitability for both laboratory and industrial applications.

From an environmental perspective, N-(3-FORMYLPHENYL)-4-METHOXYBENZAMIDE has been studied for its biodegradability and eco-friendly properties. A 2021 study published in *Environmental Science & Technology* revealed that the compound undergoes rapid degradation under aerobic conditions, making it a more sustainable option compared to traditional synthetic compounds. This attribute is particularly valuable in the context of increasing global concerns over chemical pollution and environmental sustainability.

In conclusion, N-(3-FORMYLPHENYL)-4-METHOXYBENZAMIDE (CAS No: 885459-73-4) stands out as a versatile compound with diverse applications across multiple scientific disciplines. Its unique chemical structure, combined with recent advancements in synthesis and application studies, positions it as a key player in future innovations within pharmacology, materials science, and environmental chemistry. As research continues to uncover its full potential, this compound is poised to make significant contributions to both academic and industrial sectors.

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