• 1. Examination of deposit in commercial diluted phosphoric acid
  Analyst, 1880,5, 146-147
• 2. Ester-mediated peptide formation promoted by deep eutectic solvents: a facile pathway to proto-peptides?
  Chen-Yu Chien,Sheng-Sheng Yu Chem. Commun., 2020,56, 11949-11952
• 3. Excitation dependent bidirectional electron transfer in phthalocyanine-functionalised MoS2 nanosheets?
  Christopher J. Harrison,Kyle J. Berean,Enrico Della Gaspera,Jian Zhen Ou,Richard B. Kaner,Kourosh Kalantar-zadeh,Torben Daeneke Nanoscale, 2016,8, 16276-16283
• 4. Fe(ii)-Assisted one-pot synthesis of ultra-small core–shell Au–Pt nanoparticles as superior catalysts towards the HER and ORR?
  Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
• 5. Emerging investigators
  Polym. Chem., 2015,6, 5501-5502

Introduction to 3-decyl-1-methyl-1H-imidazol-3-ium Trifluoromethanesulfonate (CAS No. 412009-62-2)

3-decyl-1-methyl-1H-imidazol-3-ium Trifluoromethanesulfonate, identified by its CAS number 412009-62-2, is a specialized ionic compound that has garnered significant attention in the field of pharmaceutical and materials science research. This compound belongs to the class of imidazolium-based cations, which are widely recognized for their versatile applications in catalysis, polymer chemistry, and medicinal chemistry. The trifluoromethanesulfonate anion (TfO-) enhances the compound's stability and reactivity, making it a valuable intermediate in synthetic chemistry.

The structure of 3-decyl-1-methyl-1H-imidazol-3-ium Trifluoromethanesulfonate consists of a 1H-imidazolium core substituted with a decyl alkyl group at the 1-position and a methyl group at the 3-position. This particular arrangement imparts unique physicochemical properties, such as high lipophilicity and thermal stability, which are critical for its utility in various applications. The presence of the trifluoromethanesulfonate moiety further contributes to its solubility in both polar and nonpolar solvents, broadening its applicability in synthetic protocols.

In recent years, 3-decyl-1-methyl-1H-imidazol-3-ium Trifluoromethanesulfonate has been extensively studied for its potential in drug development and material science. Its imidazolium scaffold is a common motif in pharmaceuticals, where it serves as a key structural element in bioactive molecules. The compound's ability to act as a ligand or catalyst in transition metal-catalyzed reactions has opened new avenues for efficient synthetic methodologies. For instance, it has been employed in the synthesis of complex organic molecules through cross-coupling reactions, highlighting its role as a versatile building block in medicinal chemistry.

One of the most compelling aspects of 3-decyl-1-methyl-1H-imidazol-3-ium Trifluoromethanesulfonate is its application in polymer chemistry. The imidazolium cation can be incorporated into ionic liquids or used as a monomer precursor for the synthesis of novel functional polymers. These polymers exhibit enhanced mechanical strength, thermal resistance, and chemical stability, making them suitable for advanced material applications such as coatings, adhesives, and electronic components. The decyl chain provides hydrophobicity, while the trifluoromethanesulfonate anion ensures excellent solubility and processability.

Recent advancements in pharmaceutical research have demonstrated the potential of 3-decyl-1-methyl-1H-imidazol-3-ium Trifluoromethanesulfonate as an intermediate in the synthesis of bioactive compounds. Its structural features allow for facile modifications at multiple positions, enabling the creation of diverse pharmacophores. Researchers have explored its use in developing novel antimicrobial agents, where the compound's ability to disrupt bacterial cell membranes has shown promising results. Additionally, its incorporation into drug delivery systems has been investigated for improving bioavailability and targeted release profiles.

The compound's stability under various conditions makes it an attractive candidate for industrial applications. For example, it has been utilized in high-performance liquid chromatography (HPLC) as a stationary phase due to its robustness and selectivity. Its compatibility with a wide range of solvents also facilitates its use in industrial-scale reactions where compatibility with organic solvents is crucial. Furthermore, the environmental profile of 3-decyl-1-methyl-1H-imidazol-3-ium Trifluoromethanesulfonate is favorable, with low toxicity and biodegradability ratings that align with green chemistry principles.

In conclusion,3-decyl-1-methyl-1H-imidazol-3-ium Trifluoromethanesulfonate (CAS No. 412009-62-2) is a multifaceted compound with significant potential across multiple scientific disciplines. Its unique structural features and functional properties make it indispensable in pharmaceutical research, polymer chemistry, and materials science. As ongoing studies continue to uncover new applications for this compound,its importance is expected to grow further, driving innovation and progress in these fields.

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