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Structure of 800402-06-6
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6-Chloro-3-iodopyridin-2-amine features a halogenated pyridine core with complementary chlorine and iodine substituents at C6 and C3, respectively. This configuration enables selective cross-coupling reactions in transition-metal catalysis, particularly in late-stage functionalization of pharmaceutical scaffolds. The electron-deficient pyridine ring enhances reactivity in Pd-catalyzed coupling processes while maintaining stability under standard reaction conditions.
6-Chloro-3-iodopyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The chlorine and iodine substituents allow sequential functionalization, while the pyridin-2-amine moiety provides a handle for further derivatization. This compound exhibits good bench stability and facilitates efficient synthesis of complex heterocyclic scaffolds relevant to pharmaceutical development.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: