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  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
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  Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzamides
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoic acids and derivatives Benzamides

3-Amino-N-(1-phenylethyl)benzamide (CAS No. 85592-79-6): A Comprehensive Overview of Its Properties and Applications

3-Amino-N-(1-phenylethyl)benzamide, with the CAS No. 85592-79-6, is a specialized organic compound that has garnered significant attention in the fields of pharmaceutical research and chemical synthesis. This compound, often referred to by its systematic name or CAS number, is a key intermediate in the development of bioactive molecules. Its unique structure, featuring an amino group and a benzamide moiety, makes it a versatile building block for drug discovery and material science applications.

The growing interest in 3-Amino-N-(1-phenylethyl)benzamide is driven by its potential role in addressing modern healthcare challenges, such as the development of novel therapeutics for chronic diseases. Researchers are particularly intrigued by its pharmacophore properties, which could be leveraged to design molecules targeting specific biological pathways. In the era of precision medicine and AI-driven drug discovery, compounds like this are invaluable for their ability to serve as scaffolds for high-throughput screening and structure-activity relationship (SAR) studies.

From a chemical perspective, 3-Amino-N-(1-phenylethyl)benzamide exhibits notable stability and solubility characteristics, making it suitable for various synthetic protocols. Its molecular weight and logP value are critical parameters for researchers optimizing drug-like properties. Recent advancements in green chemistry have also highlighted the importance of such intermediates in reducing the environmental footprint of pharmaceutical manufacturing, aligning with global sustainability goals.

In addition to its pharmaceutical applications, 3-Amino-N-(1-phenylethyl)benzamide is explored in material science for the development of advanced polymers and coatings. Its aromatic amine functionality allows for cross-linking reactions, enhancing the durability and performance of synthetic materials. This dual utility in both life sciences and industrial chemistry underscores its broad relevance.

For those searching for "3-Amino-N-(1-phenylethyl)benzamide synthesis methods" or "CAS 85592-79-6 suppliers," it’s essential to note that this compound is typically available through specialized chemical vendors. Quality control, including HPLC purity and NMR validation, is crucial when sourcing it for research purposes. Furthermore, discussions on platforms like ResearchGate and PubMed often highlight its potential in peptide mimetics and small-molecule inhibitors, reflecting its interdisciplinary appeal.

As the scientific community continues to explore the boundaries of chemical biology, 3-Amino-N-(1-phenylethyl)benzamide remains a compound of interest. Its integration into combinatorial chemistry libraries and drug development pipelines exemplifies its enduring value. Whether you’re a medicinal chemist, a materials engineer, or a biotech innovator, understanding this compound’s properties can open doors to groundbreaking applications.

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