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Structure of 1334136-60-5
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5-Bromo-2-chloro-3-nitropyridin-4-amine features a pyridine core functionalized with bromo, chloro, and nitro groups at strategic positions, enabling direct incorporation into cross-coupling and cyclization workflows. The electron-deficient aromatic framework supports efficient metal-catalyzed transformations, while the amine handle facilitates downstream derivatization in medicinal chemistry and materials synthesis.
5-Bromo-2-chloro-3-nitropyridin-4-amine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its compatible halogen functionalities. The nitro group facilitates selective reductions and further functionalization, while the amino handle allows for derivatization via acylation or coupling. Its bench-stable nature and orthogonal reactivity profile support efficient, multi-step synthetic sequences in medicinal chemistry and agrochemical development.
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: