CAS · 1260663-93-1
Product Overview
6-chloro-2,7-naphthyridin-1(2H)-one is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.
Product Specifications
| Purity | 97% min |
|---|---|
| Appearance | Yellow solid |
Applications
6-chloro-2,7-naphthyridin-1(2H)-one is primarily used as a heterocyclic intermediate in pharmaceutical research and organic synthesis. It serves as a building block for the development of bioactive compounds, including kinase inhibitors, antimicrobial agents, and other therapeutic candidates targeting nucleic acid or enzyme pathways. In medicinal chemistry, it is applied to explore structure–activity relationships, optimize pharmacokinetic properties, and design novel drug candidates based on the naphthyridine scaffold. The compound is also employed in organic synthesis to study heterocyclic reactivity, functionalization strategies, and selective substitution reactions, making it valuable in both academic and industrial research for the creation of complex molecules.
Benefits
6-chloro-2,7-naphthyridin-1(2H)-one offers several advantages that enhance its utility in chemical and pharmaceutical applications. The chloro-substituted naphthyridinone structure provides a reactive site for cross-coupling, nucleophilic substitution, and other derivatization reactions, enabling efficient synthesis of diverse derivatives. Its heterocyclic framework imparts structural rigidity and bioactive potential, supporting the design of potent and selective molecules. The compound's chemical stability allows reliable handling, storage, and reproducibility in multi-step syntheses. Additionally, its versatility as an intermediate facilitates rapid exploration of functionalized derivatives for drug discovery and materials research.
Conclusion
6-chloro-2,7-naphthyridin-1(2H)-one is a valuable heterocyclic intermediate with applications in pharmaceuticals, medicinal chemistry, and organic synthesis. Its reactive chloro group, rigid naphthyridine scaffold, and chemical stability make it a versatile building block for the development of bioactive molecules and complex derivatives. Overall, it supports efficient synthesis, drug discovery, and advanced chemical research.
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