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Structure of 53180-92-0
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5-Chloropyridazin-4-amine is a bench-stable heterocyclic amine featuring a chlorine substituent at the 5-position and a primary amine at the 4-position. This configuration enables direct functionalization in cross-coupling reactions and facilitates integration into bioactive scaffolds. The electron-deficient pyridazinone core enhances reactivity in nucleophilic substitution processes.
5-Chloropyridazin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridazinone-based scaffolds through nucleophilic substitution and coupling reactions. Its chlorine atom at the 5-position provides high reactivity for transition-metal-catalyzed cross-couplings, while the amino group at C4 offers direct functionality for derivatization. Bench-stable and readily purified by recrystallization, it facilitates scalable synthesis of bioactive heterocycles relevant to pharmaceutical development.
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Lot numbers can be found on the outside label of a product: