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Structure of 1632286-25-9
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4-Chlorocinnolin-6-amine features a chlorinated cinnolinyl core with a primary amine at the 6-position, enabling direct functionalization in heterocyclic synthesis. This electron-deficient scaffold integrates readily into pharmaceutical intermediates and advanced materials, offering enhanced reactivity under standard coupling conditions.
4-Chlorocinnolin-6-amine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C4 position via palladium-catalyzed cross-coupling reactions. Its cinnolin-6-amine core provides a rigid, electron-rich heterocyclic scaffold suitable for target-oriented synthesis. The chloro substituent offers high reactivity in Suzuki, Stille, and Buchwald-Hartwig coupling protocols, facilitating rapid diversification. Bench-stable and readily purified by flash chromatography, it functions efficiently in multi-step sequences and API development workflows.
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Lot numbers can be found on the outside label of a product: