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Structure of 2587-02-2
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2,6-Dichloro-4-pyridinamine serves as a key heterocyclic building block for pharmaceutical intermediates and agrochemical synthesis. The molecule features two electron-withdrawing chlorine substituents at the 2- and 6-positions, enhancing electrophilicity at the 4-position where the amino group is anchored. This configuration enables efficient coupling reactions under mild conditions. The compound exhibits bench-stable handling characteristics and compatibility with diverse reaction systems.
2,6-Dichloro-4-pyridinamine serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via palladium-catalyzed cross-coupling reactions. Its dual chlorine substituents provide orthogonal reactivity for sequential functionalization, while the primary amine facilitates derivatization and conjugation. Bench-stable and readily purified, it functions effectively in medicinal chemistry and agrochemical research workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: