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  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Piperidines Piperidines
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Piperidines

Exploring the Chemistry and Applications of N-Methyl-2-(4-methylpiperidin-1-yl)ethanamine (CAS No. 915924-43-5)

In the realm of organic chemistry, N-Methyl-2-(4-methylpiperidin-1-yl)ethanamine (CAS No. 915924-43-5) stands out as a compound of significant interest due to its unique structural properties and potential applications. This tertiary amine, featuring a piperidine ring and an ethylamine side chain, has garnered attention in pharmaceutical research, material science, and specialty chemical synthesis. Its molecular framework, which includes a methylpiperidine moiety, contributes to its versatility in drug design and chemical modifications.

The compound’s systematic name, N-Methyl-2-(4-methylpiperidin-1-yl)ethanamine, reflects its precise chemical architecture. Researchers often explore its physicochemical properties, such as solubility, boiling point, and stability, to optimize its use in various formulations. Recent studies highlight its role as a building block in the synthesis of more complex molecules, particularly those targeting neurological and metabolic pathways. The presence of both amine and piperidine functional groups allows for diverse reactivity, making it a valuable intermediate in medicinal chemistry.

One of the trending topics in the scientific community is the search for sustainable synthetic routes for compounds like N-Methyl-2-(4-methylpiperidin-1-yl)ethanamine. With growing emphasis on green chemistry, researchers are investigating catalytic methods and solvent-free reactions to produce this compound efficiently. Questions such as "How can CAS No. 915924-43-5 be synthesized with minimal environmental impact?" or "What are the latest advancements in piperidine-based amine applications?" frequently appear in academic forums and search engines, reflecting the compound’s relevance.

From an industrial perspective, N-Methyl-2-(4-methylpiperidin-1-yl)ethanamine is often discussed in the context of high-value intermediates. Its derivatives are explored for their potential in agrochemicals, coatings, and even specialty polymers. The compound’s ability to act as a ligand or modulator in coordination chemistry further expands its utility. For instance, its incorporation into metal-organic frameworks (MOFs) has been studied for gas storage and separation technologies, aligning with the global push for cleaner energy solutions.

Safety and regulatory compliance are also critical considerations when working with CAS No. 915924-43-5. While not classified as hazardous under standard guidelines, proper handling protocols—such as the use of personal protective equipment (PPE) and adequate ventilation—are recommended. Researchers often inquire about "Material Safety Data Sheet (MSDS) for N-Methyl-2-(4-methylpiperidin-1-yl)ethanamine" or "Best practices for storing amine-based compounds", underscoring the importance of responsible usage.

In summary, N-Methyl-2-(4-methylpiperidin-1-yl)ethanamine (CAS No. 915924-43-5) exemplifies the intersection of innovation and practicality in modern chemistry. Its structural features, coupled with its broad applicability, make it a subject of ongoing research and industrial interest. As scientific inquiries evolve, this compound will likely remain a focal point for advancements in drug discovery, materials engineering, and sustainable synthesis methodologies.

• 355144-95-5(2-4-(propan-2-yl)piperidin-1-ylethan-1-amine)
• 915923-35-2(N-Ethyl-2-(4-methylpiperidin-1-yl)ethanamine)
• 876716-58-4(2-(3,5-Dimethylpiperidin-1-yl)ethanamine)
• 775288-46-5(1-methyl-4-[2-(piperidin-4-yl)ethyl]piperazine)
• 14156-95-7(2-(4-methyl-1-piperidyl)ethanamine)
• 104304-11-2(1-Azoniabicyclo[2.2.2]octane, 1,1'-(1,2-ethanediyl)bis-, dibromide)
• 67990-20-9(1,1'-ethylenebis[3-methylpiperidine])
• 775288-50-1(1H-1,4-Diazepine, hexahydro-1-methyl-4-[2-(4-piperidinyl)ethyl]-)
• 85723-75-7(2-(3-Methylpiperidin-1-yl)ethanamine)
• 1177306-60-3(2-(4-Ethylpiperidin-1-yl)ethanamine)