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• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers Anisoles

Comprehensive Overview of 2-((2-(3-Methoxyphenoxy)ethyl)amino)ethanol (CAS No. 420104-03-6)

2-((2-(3-Methoxyphenoxy)ethyl)amino)ethanol, with the CAS number 420104-03-6, is a specialized organic compound that has garnered significant attention in pharmaceutical and chemical research. This compound, characterized by its unique phenoxyethylaminoethanol structure, is often explored for its potential applications in drug development and material science. The presence of both methoxy and aminoethanol functional groups makes it a versatile intermediate for synthesizing more complex molecules.

In recent years, the demand for bioactive intermediates like 2-((2-(3-Methoxyphenoxy)ethyl)amino)ethanol has surged, driven by advancements in precision medicine and green chemistry. Researchers are particularly interested in its role as a building block for designing targeted therapies, especially in neurological and cardiovascular fields. Its molecular structure allows for modifications that enhance drug bioavailability and receptor binding affinity, addressing common challenges in modern pharmacology.

The compound’s synthetic pathway often involves etherification and amination reactions, which are critical topics in organic synthesis discussions. Laboratories focusing on high-throughput screening frequently include CAS 420104-03-6 in their libraries due to its scaffold diversity. Additionally, its solubility and stability under physiological conditions make it a candidate for formulation studies, aligning with the growing trend of computational drug design.

From an industrial perspective, 2-((2-(3-Methoxyphenoxy)ethyl)amino)ethanol is valued for its scalable production potential. Manufacturers emphasize cost-effective synthesis methods to meet the needs of contract research organizations (CROs) and academic institutions. The compound’s purity standards and analytical characterization (e.g., HPLC, NMR) are rigorously documented, ensuring compliance with Good Manufacturing Practices (GMP) for preclinical applications.

Environmental and safety considerations are also integral to its use. While not classified as hazardous, proper handling protocols are recommended to maintain laboratory safety. The compound’s biodegradability profile is under study, reflecting the broader shift toward sustainable chemistry. This aligns with global initiatives like the UN Sustainable Development Goals (SDGs), particularly in reducing chemical waste.

In summary, 2-((2-(3-Methoxyphenoxy)ethyl)amino)ethanol (CAS 420104-03-6) represents a convergence of pharmaceutical innovation and industrial applicability. Its relevance to drug discovery, coupled with environmental consciousness, positions it as a compound of enduring scientific and commercial interest.

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