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Structure of 915006-52-9
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6-Bromo-2-iodopyridin-3-amine features a pyridine core functionalized with bromo and iodo groups at the 6- and 2-positions, respectively, and an amine substituent at the 3-position. This tri-functionalized scaffold enables direct coupling in cross-coupling reactions, particularly Pd-catalyzed variants, where the iodide serves as a high-reactivity handle. The molecule exhibits robust stability under standard bench conditions, facilitating straightforward handling in synthetic workflows.
6-Bromo-2-iodopyridin-3-amine serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heterocyclic scaffolds. The ortho-halogen substitution pattern facilitates sequential functionalization, while the amino group provides a handle for derivatization. Bench-stable and compatible with standard reaction conditions, it supports scalable synthesis of complex nitrogen-containing architectures relevant to medicinal chemistry and materials science.
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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: