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Structure of 61070-99-3
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Pyridazine-3,6-diamine delivers a highly reactive diamino scaffold for constructing functionalized heterocycles. This bench-stable compound features two nitrogen-rich amine groups positioned at the 3 and 6 positions of the pyridazine core, enabling efficient coupling reactions and integration into bioactive molecules.
Pyridazine-3,6-diamine serves as a versatile building block in medicinal chemistry and materials science, enabling the synthesis of heterocyclic scaffolds through nucleophilic substitution, cycloaddition, and metal-catalyzed coupling reactions. Its dual amine functionality offers orthogonal reactivity for conjugation and derivatization, while its inherent stability under standard bench conditions facilitates purification and scale-up. Functions effectively in the construction of kinase inhibitors, antiviral agents, and functional polymers.
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Lot numbers can be found on the outside label of a product: