• 1. Dissociative dynamics of O2 on Ag(110)?
  Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
• 2. Fate of single walled carbon nanotubes in wetland ecosystems?
  Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
• 3. Evolution of important glucosinolates in three common Brassica vegetables during their processing into vegetable powder and in vitro gastric digestion
  Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220
• 4. Emergence of cationic polyamine dendrimersomes: design, stimuli sensitivity and potential biomedical applications
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• 5. Fe/Fe3C@C nanoparticles encapsulated in N-doped graphene–CNTs framework as an efficient bifunctional oxygen electrocatalyst for robust rechargeable Zn–air batteries?
  Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526

• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds N-arylamides

Comprehensive Overview of N-3-pyridinyl-Formamide (CAS No. 22236-96-0): Properties, Applications, and Industry Insights

N-3-pyridinyl-Formamide (CAS No. 22236-96-0) is a specialized organic compound widely recognized for its versatile applications in pharmaceutical research, agrochemical development, and material science. This compound, characterized by its pyridine and formamide functional groups, has garnered significant attention due to its unique chemical properties and potential in synthesizing high-value intermediates. In this article, we delve into its molecular structure, synthesis methods, and emerging trends aligned with current industry demands.

The molecular formula of N-3-pyridinyl-Formamide is C₆H₆N₂O, with a molar mass of 122.13 g/mol. Its structure features a pyridine ring linked to a formamide group, which contributes to its polarity and solubility in common organic solvents like ethanol and dimethyl sulfoxide (DMSO). These properties make it a valuable building block in heterocyclic chemistry, particularly in the design of drug candidates and catalytic ligands.

Recent studies highlight the role of CAS No. 22236-96-0 in green chemistry initiatives, where researchers explore solvent-free synthesis routes to minimize environmental impact. This aligns with the growing demand for sustainable chemical processes, a topic frequently searched in academic and industrial databases. Additionally, its potential as a corrosion inhibitor in industrial applications has sparked interest, addressing concerns about material longevity in harsh environments.

In the pharmaceutical sector, N-3-pyridinyl-Formamide derivatives are investigated for their bioactivity, particularly in targeting enzyme pathways associated with metabolic disorders. This connects to trending searches like "pyridine-based drug discovery" and "small molecule therapeutics." Analytical techniques such as NMR, HPLC, and mass spectrometry are routinely employed to validate its purity, ensuring compliance with regulatory standards for high-precision applications.

From a commercial perspective, suppliers of CAS No. 22236-96-0 emphasize batch-to-batch consistency and scalability, responding to queries about bulk procurement and custom synthesis. Storage recommendations typically include protection from moisture and light, with stability data supporting long-term usability under controlled conditions. These practical insights cater to frequent user questions regarding handling protocols and shelf-life optimization.

Looking ahead, innovations in catalytic amidation and microwave-assisted synthesis may further enhance the production efficiency of N-3-pyridinyl-Formamide. Such advancements resonate with industry professionals searching for process intensification strategies. As research continues, this compound is poised to remain relevant in interdisciplinary applications, bridging gaps between academic discovery and industrial implementation.

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