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Structure of 215364-85-5
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3-Bromo-2-chloropyridin-4-amine features a pyridine core functionalized with bromo and chloro substituents at the 3- and 2-positions, respectively, and an amine group at the 4-position. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, enabling direct coupling reactions via its amine handle. The dual halogenation pattern supports sequential cross-coupling strategies in target diversification.
3-Bromo-2-chloropyridin-4-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 efficient Suzuki, Stille, or Negishi couplings, while the chloro and amino functionalities provide sites for further functionalization. Its bench-stable nature and compatibility with standard synthetic protocols make it ideal for constructing complex heterocyclic scaffolds in API development.
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GHS Pictogram :
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GHS No : GHS05,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-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: