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Structure of 36258-82-9
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4-Chloro-3H-[1,2,3]triazolo[4,5-c]pyridine is a heterocyclic scaffold featuring a chlorinated triazolopyridine core with enhanced electron-deficient character. This rigid, planar structure facilitates π-stacking interactions and integrates readily into bioactive molecules. The chlorine substituent enables site-specific functionalization via palladium-catalyzed coupling reactions, making it valuable for medicinal chemistry and materials synthesis.
4-Chloro-3H-[1,2,3]triazolo[4,5-c]pyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient construction of triazolopyridine scaffolds. Its chlorine substituent facilitates nucleophilic substitution reactions, supporting the synthesis of diverse analogs through coupling with amines, thiols, and other nucleophiles. The compound exhibits good bench stability and compatibility with standard purification methods, making it well-suited for iterative synthetic workflows in API development.
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Lot numbers can be found on the outside label of a product: