• 1. Examination of the hydrogen-bonding networks in small water clusters (n = 2–5, 13, 17) using absolutely localized molecular orbital energy decomposition analysis?
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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Quinolines and derivatives Quinolines and derivatives
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Quinolines and derivatives

Ethyl[(quinolin-2-yl)methyl]amine (CAS No. 680591-03-1): A Versatile Chemical Compound with Emerging Applications

Ethyl[(quinolin-2-yl)methyl]amine (CAS No. 680591-03-1) is a specialized organic compound that has garnered significant attention in recent years due to its unique structural properties and potential applications across various industries. This quinoline derivative combines the aromatic characteristics of quinoline with the reactivity of an ethylamine group, making it a valuable intermediate in pharmaceutical research, material science, and specialty chemical synthesis.

The molecular structure of ethyl[(quinolin-2-yl)methyl]amine features a quinoline core with an ethylamino substituent at the 2-position, which contributes to its distinctive chemical behavior. Researchers have particularly focused on this compound's potential as a building block for more complex molecules, especially in the development of novel pharmaceutical intermediates and functional materials. Recent studies suggest that derivatives of this compound may exhibit interesting biological activities, though further research is needed to fully explore these possibilities.

In the pharmaceutical sector, ethyl[(quinolin-2-yl)methyl]amine has shown promise as a precursor for drug discovery programs. The quinoline moiety is known to interact with various biological targets, while the ethylamine group provides opportunities for further structural modifications. This dual functionality makes the compound particularly valuable for medicinal chemists working on targeted therapies and small molecule drugs. Current research trends indicate growing interest in its potential applications in neurological and anti-inflammatory research areas.

The material science community has also taken notice of ethyl[(quinolin-2-yl)methyl]amine (CAS No. 680591-03-1) due to its potential in creating novel functional materials. The compound's aromatic system and amine functionality make it suitable for incorporation into coordination polymers and metal-organic frameworks (MOFs). These applications align with current industry demands for advanced materials with tailored properties for energy storage, catalysis, and sensing technologies.

From a synthetic chemistry perspective, ethyl[(quinolin-2-yl)methyl]amine offers several advantages. The compound demonstrates good stability under standard conditions while maintaining sufficient reactivity for further transformations. This balance makes it particularly useful for multi-step synthesis processes. Recent publications have highlighted its role in heterocyclic chemistry and as a ligand in catalytic systems, reflecting the compound's versatility in modern synthetic methodologies.

The commercial availability of ethyl[(quinolin-2-yl)methyl]amine has improved in recent years, with several specialty chemical suppliers now offering this compound in various quantities. Market analysis suggests growing demand from both academic research institutions and industrial R&D departments. Quality control remains a critical factor, with HPLC purity typically exceeding 95% for research-grade material. Storage recommendations generally suggest keeping the compound in a cool, dry environment protected from light to maintain stability.

Safety considerations for handling ethyl[(quinolin-2-yl)methyl]amine follow standard laboratory protocols for organic compounds. While not classified as highly hazardous, proper personal protective equipment including gloves and eye protection is recommended when working with this chemical. The compound's material safety data sheet (MSDS) provides detailed handling instructions that should be reviewed prior to use. Environmental impact studies indicate that the compound should be treated as standard organic waste following local regulations.

Recent advancements in green chemistry have explored more sustainable synthesis routes for ethyl[(quinolin-2-yl)methyl]amine and related compounds. Researchers are investigating catalytic methods and alternative solvents to reduce the environmental footprint of production processes. These developments align with broader industry trends toward sustainable chemical manufacturing and could potentially lower production costs while improving scalability.

Analytical characterization of ethyl[(quinolin-2-yl)methyl]amine typically involves standard techniques including NMR spectroscopy, mass spectrometry, and HPLC analysis. The compound's distinct spectral features facilitate quality control and purity assessment. Recent publications have also reported the use of advanced techniques like X-ray crystallography to determine its solid-state structure, providing valuable insights for material science applications.

The future outlook for ethyl[(quinolin-2-yl)methyl]amine (CAS No. 680591-03-1) appears promising, with potential applications continuing to emerge across multiple disciplines. As research into quinoline-based compounds expands, this particular derivative may find new roles in areas such as organic electronics, advanced catalysis, and bioconjugation chemistry. The compound's combination of structural features and synthetic accessibility positions it as a valuable tool for both academic and industrial researchers.

For researchers considering working with ethyl[(quinolin-2-yl)methyl]amine, current literature suggests several promising directions. These include exploring its potential as a pharmacophore in drug design, investigating its coordination chemistry with transition metals, and developing novel synthetic methodologies utilizing its unique reactivity. The compound's growing presence in scientific literature indicates that it may become increasingly important in specialized chemical research in the coming years.

• 217808-43-0(rac 4-Amino Deprenyl)
• 27114-20-1(1,2-Ethanediamine,N1,N1-diethyl-N2-(2-quinolinylmethyl)-, hydrochloride (1:3))
• 484671-42-3(1,2-ETHANEDIAMINE, N-METHYL-N-(2-QUINOLINYLMETHYL)-)
• 90936-75-7(N~1~-[(Quinolin-2-yl)methyl]propane-1,3-diamine)
• 566189-49-9(1,10-PHENANTHROLINE-2,9-DIMETHANAMINE, N,N'-BIS[2-(ETHYLAMINO)ETHYL]-)
• 1189651-22-6(2-(Diethylamino)methyl-13Cindole)
• 89292-71-7(Quinoline, 2-(1-piperazinylmethyl)-, hydrochloride (1:3))
• 90888-62-3((1H-Indol-2-ylmethyl)methylamine)
• 136727-11-2(N-Methyl-1-quinolin-2-ylmethanamine)
• 83852-37-3(2-QUINOLINEMETHANAMINE, N,N-DIETHYL-)