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Structure of 130284-52-5
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6-Bromo-5-chloropyridin-3-amine features a pyridine core functionalized with bromo and chloro substituents at the 6- and 5-positions, respectively, and an amine group at C3. This electron-deficient heterocycle enables direct coupling in cross-coupling reactions, serving as a key building block for pharmaceutical intermediates and agrochemical scaffolds. The molecule exhibits good stability under standard handling conditions.
6-Bromo-5-chloropyridin-3-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromo group facilitates Suzuki-Miyaura and Buchwald-Hartwig couplings, while the chloro substituent offers stability under standard reaction conditions. Its primary amine functionality supports direct derivatization or incorporation into heterocyclic scaffolds. The compound exhibits good bench stability and is readily purified by silica gel chromatography, making it suitable for iterative synthesis workflows in API 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: