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Structure of 166047-15-0
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5-Bromo-N3-methylpyridine-2,3-diamine features a pyridine core functionalized with bromo, methylamino, and diamino groups, enabling versatile coupling in transition metal-catalyzed reactions. The electron-rich diaminopyridine scaffold supports efficient coordination to metals, while the bromo substituent facilitates cross-coupling transformations. This bench-stable derivative integrates readily into complex heterocyclic architectures for medicinal chemistry and materials applications.
5-Bromo-N3-methylpyridine-2,3-diamine serves as a versatile building block for the synthesis of bioactive heterocycles, enabling efficient Pd-catalyzed cross-coupling and cyclization reactions. The bromo group facilitates direct functionalization, while the N3-methylated diamine moiety offers enhanced stability and orthogonal reactivity. This compound functions effectively in constructing complex scaffolds relevant to medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS07,GHS05
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Signal Word : Danger
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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-H312-H315-H318-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P354+P338-P317-P319-P330-P332+P317-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: