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  Gerald J. Meyer,Leif Hammarstr?m Chem. Sci., 2020,11, 3460-3473
• 2. Examination of the hydrogen-bonding networks in small water clusters (n = 2–5, 13, 17) using absolutely localized molecular orbital energy decomposition analysis?
  Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
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  Chen-Yu Chien,Sheng-Sheng Yu Chem. Commun., 2020,56, 11949-11952
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• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Aralkylamines
• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Amines Aralkylamines

N-(1-Ethyl-1H-pyrazol-4-yl)methylethanamine Hydrochloride (CAS 1269104-94-0): A Comprehensive Overview

N-(1-Ethyl-1H-pyrazol-4-yl)methylethanamine Hydrochloride (CAS 1269104-94-0) is a specialized chemical compound that has garnered significant attention in pharmaceutical and biochemical research. This pyrazole derivative is known for its unique structural properties, making it a valuable intermediate in the synthesis of various bioactive molecules. Researchers and industry professionals often search for "N-(1-Ethyl-1H-pyrazol-4-yl)methylethanamine Hydrochloride uses" or "CAS 1269104-94-0 applications," reflecting its growing relevance in modern chemistry.

The compound features a pyrazole ring substituted with an ethyl group and an ethanamine moiety, which is protonated as a hydrochloride salt. This structural configuration enhances its solubility and stability, making it suitable for various experimental and industrial applications. Recent trends show increased interest in "pyrazole-based compounds in drug discovery," aligning with the compound's potential in medicinal chemistry. Its molecular formula and precise physicochemical properties are critical for researchers optimizing synthetic pathways or designing new molecular entities.

One of the most searched questions related to this compound is "How to synthesize N-(1-Ethyl-1H-pyrazol-4-yl)methylethanamine Hydrochloride?" The synthesis typically involves the reaction of 1-ethyl-1H-pyrazole-4-carbaldehyde with methylamine, followed by reduction and salt formation. The process highlights the compound's role as a versatile building block in organic synthesis. Additionally, its hydrochloride salt form improves handling and storage, addressing common challenges in chemical manufacturing.

In the context of pharmaceutical research, N-(1-Ethyl-1H-pyrazol-4-yl)methylethanamine Hydrochloride is explored for its potential as a precursor in the development of central nervous system (CNS) therapeutics. The pyrazole scaffold is frequently employed in drugs targeting neurological disorders, a hot topic in 2024 due to rising global health concerns. Searches like "pyrazole derivatives in CNS drugs" or "CAS 1269104-94-0 pharmacological studies" underscore this trend.

The compound's market dynamics are also noteworthy. With increasing demand for high-purity chemical intermediates, suppliers of CAS 1269104-94-0 are focusing on scalable production methods. Quality control measures, such as HPLC and NMR analysis, ensure compliance with industry standards. Queries like "where to buy N-(1-Ethyl-1H-pyrazol-4-yl)methylethanamine Hydrochloride" reflect its commercial significance.

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In summary, N-(1-Ethyl-1H-pyrazol-4-yl)methylethanamine Hydrochloride (CAS 1269104-94-0) is a multifaceted compound with broad applications in drug development and material science. Its structural versatility, coupled with evolving market needs, positions it as a key player in advanced chemical research. For researchers and suppliers alike, understanding its properties and potential is essential to leveraging its full capabilities.

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