• 1. Metal ion-promoted cleavage of mRNA 5′-cap models: hydrolysis of the triphosphate bridge and reactions of the N 7-methylguanine base
  Satu Valakoski,Suvi Heiskanen,Sanna Andersson,Mari L?hde,Satu Mikkola 7-methylguanine base. Satu Valakoski Suvi Heiskanen Sanna Andersson Mari L?hde Satu Mikkola J. Chem. Soc. Perkin Trans. 2 2002 604
• 2. (Un)suitability of the use of pH buffers in biological, biochemical and environmental studies and their interaction with metal ions – a review
  Carlos M. H. Ferreira,Isabel S. S. Pinto,Eduardo V. Soares,Helena M. V. M. Soares RSC Adv. 2015 5 30989
• 3. Wireless bipolar electrode-based textile electrofluidics: towards novel micro-total-analysis systems
  Jawairia Umar Khan,Andres Ruland,Sepidar Sayyar,Brett Paull,Jun Chen,Peter C. Innis Lab Chip 2021 21 3979
• 4. Sensing of peptide hormones with dynamic combinatorial libraries of metal–dye complexes: the advantage of time-resolved measurements
  Friederike Zaubitzer,Thomas Riis-Johannessen,Kay Severin Org. Biomol. Chem. 2009 7 4598
• 5. Detection of polyamines by an extended gate-type organic transistor functionalized with a carboxylate attached 1,3,4-thiadiazole derivative
  Koichiro Asano,Yui Sasaki,Qi Zhou,Riho Mitobe,Wei Tang,Xiaojun Lyu,Masao Kamiko,Hikaru Tanaka,Akari Yamagami,Kazutake Hagiya,Tsuyoshi Minami J. Mater. Chem. C 2021 9 11690

• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Cyclohexylamines
• Other Chemical Reagents

Introduction to Compound with CAS No. 103-47-9 and Product Name CHES

The compound with the CAS number 103-47-9 is a well-studied chemical entity that has garnered significant attention in the field of pharmaceutical chemistry and biomedicine. This compound, chemically known as N-(2-hydroxyethyl)ethanamine, is widely recognized for its versatile applications in drug development and biochemical research. The product name CHES, which stands for 2-(2-Carboxyethylamino)ethanol, is a derivative of this compound and has been extensively utilized in various scientific and industrial processes.

CHES is a crucial component in the synthesis of pharmaceutical intermediates, where its bifunctional nature—possessing both an amine and a carboxyl group—makes it an invaluable building block. The compound’s ability to participate in various chemical reactions, such as condensation, esterification, and polymerization, underscores its significance in synthetic chemistry. Recent advancements in the field have highlighted its role in the development of novel drug formulations, particularly in the area of targeted therapy and personalized medicine.

In recent years, research has demonstrated the potential of CHES as a chelating agent in metal-based drug formulations. The carboxyl group in CHES facilitates the coordination with metal ions, making it an effective ligand for creating complexes that exhibit enhanced bioavailability and reduced toxicity. This property has been particularly explored in the context of anticancer therapies, where metallo-drugs are being designed to selectively target tumor cells while minimizing side effects on healthy tissues.

The amine group in CHES also plays a pivotal role in its biological activity. Studies have shown that derivatives of CHES can modulate enzyme activity and cellular signaling pathways, making them promising candidates for treating neurological disorders and inflammatory conditions. The compound’s ability to interact with biological molecules has led to its incorporation into various experimental therapies aimed at enhancing synaptic plasticity and reducing neuroinflammation.

From a synthetic chemistry perspective, CHES serves as a key intermediate in the production of polyamides and polyesters. These polymers are not only used in textile industries but also find applications in biomedical materials, such as sutures and wound dressings. The biocompatibility and biodegradability of polymers derived from CHES make them ideal for use in medical implants and tissue engineering scaffolds.

Moreover, the compound’s role in environmental science cannot be overlooked. Researchers have been investigating the use of CHES as a corrosion inhibitor in industrial settings. Its ability to form stable complexes with metal ions helps prevent oxidative degradation of metals, thereby extending the lifespan of industrial equipment and reducing maintenance costs.

The latest studies have also explored the potential of CHES in sustainable agriculture. By acting as a soil amendment, derivatives of this compound can enhance nutrient uptake by plants while reducing soil acidity. This application aligns with global efforts to develop eco-friendly agricultural practices that minimize environmental impact.

In conclusion, the compound with CAS No. 103-47-9 and its derivative CHES represent a cornerstone in modern chemical research and industrial applications. Their multifaceted roles in pharmaceuticals, materials science, environmental protection, and agriculture underscore their importance as versatile chemical entities. As scientific understanding continues to evolve, it is expected that new applications for these compounds will emerge, further solidifying their place at the forefront of innovation.

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• 127075-47-2((S)-Pyrrolidin-2-ylmethanesulfonic acid)
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