• 1. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
  Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
• 2. Fate of Sb(v) and Sb(iii) species along a gradient of pH and oxygen concentration in the Carnoulès mine waters (Southern France)
  Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
• 3. Excimer formation effects and trap-assisted charge recombination loss channels in organic solar cells of perylene diimide dimer acceptors?
  Min Kim,Jae-Joon Lee,Tengling Ye,Panagiotis E. Keivanidis,Kilwon Cho J. Mater. Chem. C, 2020,8, 1686-1696
• 4. Elusive 2-aminofuran Diels–Alder substrates for a straightforward synthesis of polysubstituted anilines?
  Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Pyridine carboxaldehydes

Comprehensive Guide to 2-(morpholin-4-yl)pyridine-4-carbaldehyde (CAS No. 864068-87-1): Properties, Applications, and Market Insights

2-(morpholin-4-yl)pyridine-4-carbaldehyde (CAS No. 864068-87-1) is a versatile heterocyclic compound that has garnered significant attention in pharmaceutical and chemical research. This compound, featuring a pyridine-carbaldehyde core linked to a morpholine moiety, serves as a key intermediate in the synthesis of various bioactive molecules. Its unique structural properties make it valuable for drug discovery and material science applications.

The growing interest in 2-(morpholin-4-yl)pyridine-4-carbaldehyde is driven by its role in developing kinase inhibitors and other therapeutic agents. Researchers frequently search for "pyridine-carbaldehyde derivatives" and "morpholine-containing compounds" due to their relevance in targeting diseases like cancer and inflammation. This compound’s CAS No. 864068-87-1 is often queried in chemical databases, highlighting its importance in synthetic chemistry.

From a chemical perspective, 2-(morpholin-4-yl)pyridine-4-carbaldehyde exhibits notable reactivity. The aldehyde functional group allows for diverse transformations, such as condensation reactions, making it a valuable building block for organic synthesis. Additionally, the morpholine ring enhances solubility and bioavailability, which is crucial for pharmaceutical applications. These properties align with current trends in green chemistry and sustainable drug development.

In the pharmaceutical industry, 2-(morpholin-4-yl)pyridine-4-carbaldehyde is explored for its potential in designing small-molecule drugs. Its structural motif is found in compounds targeting protein kinases, which are implicated in numerous diseases. Searches for "kinase inhibitor intermediates" and "morpholine-based pharmaceuticals" often lead to this compound, reflecting its relevance in modern drug discovery pipelines.

The market for 2-(morpholin-4-yl)pyridine-4-carbaldehyde is expanding, driven by increasing demand for high-purity chemical intermediates. Suppliers and researchers prioritize compounds with CAS No. 864068-87-1 due to their consistent quality and application versatility. Recent advancements in catalytic synthesis have further optimized its production, reducing costs and environmental impact—a key concern in today’s chemical manufacturing landscape.

Beyond pharmaceuticals, 2-(morpholin-4-yl)pyridine-4-carbaldehyde finds applications in material science. Its ability to form stable complexes with metals makes it useful in coordination chemistry and catalysis. This dual utility in drug design and materials research positions it as a compound of interdisciplinary interest, answering queries like "multifunctional heterocycles" and "metal-organic frameworks."

In summary, 2-(morpholin-4-yl)pyridine-4-carbaldehyde (CAS No. 864068-87-1) is a pivotal compound bridging medicinal chemistry and advanced materials. Its structural features, coupled with growing industrial demand, ensure its continued prominence in scientific and commercial arenas. Researchers and manufacturers alike benefit from its adaptability, making it a staple in modern chemical innovation.

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