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Structure of 163452-78-6
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5-Bromo-2-chloropyridine-3,4-diamine features a pyridine core functionalized with bromo and chloro substituents at the 5- and 2-positions, respectively, flanking two diamino groups. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, enabling direct coupling reactions and facilitating access to complex nitrogen-containing scaffolds under standard conditions.
5-Bromo-2-chloropyridine-3,4-diamine serves as a versatile building block in medicinal chemistry and agrochemical synthesis. The molecule features orthogonal halogen handles (Br at C5, Cl at C2) and two primary amine groups, enabling sequential cross-coupling reactions or derivatization under standard Pd-catalyzed conditions. Its bench-stable crystalline form facilitates handling and purification, while the electron-deficient pyridine core supports diverse functional group transformations. Widely used in constructing kinase inhibitors and heterocyclic scaffolds, it functions reliably in multi-step synthetic sequences requiring selective reactivity.
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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: