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• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Amino acids, peptides, and analogues Amino acids and derivatives

Comprehensive Overview of 2-(3-Nitropyridin-2-yl)aminoacetic Acid (CAS No. 118807-77-5): Properties, Applications, and Research Insights

2-(3-Nitropyridin-2-yl)aminoacetic acid (CAS No. 118807-77-5) is a specialized organic compound with a unique molecular structure combining a nitropyridine moiety and an aminoacetic acid group. This compound has garnered significant attention in pharmaceutical and agrochemical research due to its potential as a building block for bioactive molecules. The presence of both nitro and amino functional groups makes it a versatile intermediate for synthesizing derivatives with tailored properties.

In recent years, the demand for nitropyridine derivatives like 2-(3-nitropyridin-2-yl)aminoacetic acid has surged, driven by their applications in drug discovery and material science. Researchers are particularly interested in its role as a precursor for heterocyclic compounds, which are pivotal in designing kinase inhibitors and antimicrobial agents. Its CAS number 118807-77-5 is frequently searched in chemical databases, reflecting its relevance in academic and industrial settings.

The compound’s physicochemical properties, such as solubility in polar solvents and thermal stability, have been extensively studied. Analytical techniques like HPLC and NMR spectroscopy confirm its high purity, making it suitable for high-throughput screening in drug development. Environmental and safety studies highlight its biodegradability under controlled conditions, aligning with the growing focus on green chemistry principles.

From an SEO perspective, queries like "synthesis of 2-(3-nitropyridin-2-yl)aminoacetic acid" or "CAS 118807-77-5 suppliers" rank highly, indicating user interest in procurement and synthetic protocols. The compound’s association with crop protection chemicals also ties into trending topics like sustainable agriculture. Its potential in cancer research further elevates its profile, as evidenced by peer-reviewed publications exploring its mechanistic pathways.

Innovations in catalytic reactions have streamlined the production of 2-(3-nitropyridin-2-yl)aminoacetic acid, reducing costs and waste. This aligns with industry demands for cost-effective intermediates. Regulatory compliance, such as REACH and FDA guidelines, ensures its safe handling, a common concern among laboratory professionals. Future research may explore its structure-activity relationships to unlock novel therapeutic applications.

In summary, 2-(3-nitropyridin-2-yl)aminoacetic acid (CAS No. 118807-77-5) exemplifies the intersection of chemistry and innovation. Its multifaceted utility in life sciences and compatibility with automated synthesis platforms position it as a compound of enduring scientific and commercial value.

• 866010-53-9(N-(2-Methoxyethyl)-3-nitro-2-pyridinamine)
• 90559-63-0(ethyl 2-(3-nitropyridin-2-yl)aminoacetate)
• 252954-49-7(Ethanol,2-[(6-amino-5-nitro-2-pyridinyl)amino]-)
• 61100-29-6(2,6-Pyridinediamine, N,N'-bis(2-methoxyethyl)-3-nitro-)
• 50798-38-4(2-(3-nitropyridin-2-yl)aminoethanol Hydrochloride)
• 3264-08-2(Glycine,N-(3,5-dinitro-2-pyridinyl)-)
• 26820-65-5(2-Ethylamino-3-nitropyridine)
• 98279-88-0(2-(5-nitropyridin-2-yl)aminoacetic Acid)
• 116059-08-6(Glycine, N-(3,5-dinitro-2-pyridinyl)-N-methyl-, ethyl ester)
• 57461-53-7(methyl 2-(3-nitropyridin-2-ylamino)acetate)