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Structure of 400777-06-2
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6-Chloro-2-iodopyridin-3-amine features a strategically positioned chloro group and iodine handle, enabling selective cross-coupling reactions in medicinal chemistry. The electron-deficient pyridine core enhances reactivity in palladium-catalyzed transformations, while the amine functionality offers direct derivatization potential. This bench-stable scaffold integrates efficiently into complex heterocyclic architectures under standard conditions.
6-Chloro-2-iodopyridin-3-amine serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient access to functionalized pyridine scaffolds. The ortho-chloro and iodo substituents provide complementary reactivity for sequential coupling, while the amino group offers direct derivatization potential. Bench-stable and compatible with standard reaction conditions, it facilitates rapid assembly of complex heterocyclic architectures in medicinal chemistry and materials science applications.
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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: