• 1. An insight into the hybridization mechanism of hairpin DNA physically immobilized on chemically modified graphenes
  Adeline Huiling Loo,Alessandra Bonanni,Martin Pumera Analyst, 2013,138, 467-471
• 2. An Appraisal of pH triggered Bacitracin drug release, through composite hydrogel systems
  RabailGul,MariamMir,MurtazaNAli
• 3. An algal process treatment combined with the Fenton reaction for high concentrations of amoxicillin and cefradine
  Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
• 4. Acentric and chiral heterometallic inorganic–organic hybrid frameworks mediated by alkali or alkaline earth ions: synthesis and NLO properties
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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Halopyridines Polyhalopyridines

Comprehensive Analysis of 1-(2-Chloropyridin-4-yl)ethan-1-amine dihydrochloride (CAS No. 2250243-31-1)

The compound 1-(2-Chloropyridin-4-yl)ethan-1-amine dihydrochloride (CAS No. 2250243-31-1) has garnered significant attention in the pharmaceutical and agrochemical industries due to its versatile applications. As a chloropyridine derivative, it serves as a key intermediate in the synthesis of various bioactive molecules. Researchers and manufacturers are increasingly exploring its potential in drug discovery, particularly in the development of kinase inhibitors and antiviral agents, aligning with the growing demand for novel therapeutics.

In recent years, the search for small-molecule modulators has surged, with 1-(2-Chloropyridin-4-yl)ethan-1-amine dihydrochloride emerging as a valuable building block. Its structural features, including the chloropyridine core and amine functionality, make it a prime candidate for structure-activity relationship (SAR) studies. This compound is often referenced in patents and scientific literature related to cancer research and central nervous system (CNS) disorders, addressing pressing global health challenges.

The synthesis and optimization of CAS 2250243-31-1 have been refined to meet the demands of high-throughput screening and combinatorial chemistry. Its dihydrochloride salt form enhances solubility, a critical factor in bioavailability studies. Laboratories focusing on medicinal chemistry frequently inquire about its purity, stability, and scalability—topics that dominate forums and academic discussions. This aligns with the broader industry shift toward green chemistry and sustainable synthesis methods.

Beyond pharmaceuticals, 1-(2-Chloropyridin-4-yl)ethan-1-amine dihydrochloride finds utility in agrochemical formulations. Its role in developing crop protection agents resonates with the urgent need for food security solutions. As climate change impacts agricultural productivity, researchers are investigating its derivatives for pest resistance and plant growth regulation. This dual applicability in human health and agriculture underscores its economic and scientific relevance.

Analytical techniques such as HPLC, NMR, and mass spectrometry are routinely employed to characterize CAS 2250243-31-1. Quality control protocols emphasize the importance of low impurity profiles, especially for GMP-grade production. The compound’s storage conditions and handling guidelines are frequently searched topics, reflecting the precision required in modern laboratories. These discussions often intersect with broader trends like lab automation and digital data management.

In summary, 1-(2-Chloropyridin-4-yl)ethan-1-amine dihydrochloride represents a critical junction between chemical innovation and applied science. Its multifaceted applications, coupled with rigorous research, position it as a compound of enduring interest. As industries evolve toward precision medicine and sustainable agriculture, this molecule will likely remain at the forefront of scientific inquiry and industrial application.

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