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Structure of 1206249-65-1
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6-Bromo-4-chloropyridin-2-amine features a pyridine core functionalized with bromo and chloro substituents at the 6- and 4-positions, respectively, and an amino group at the 2-position. This electron-deficient heterocycle serves as a key building block in medicinal chemistry for constructing kinase inhibitors and bioactive scaffolds. The molecule exhibits enhanced reactivity in palladium-catalyzed cross-coupling reactions due to the orthogonal halogenation pattern, enabling selective functionalization. Its bench-stable nature facilitates handling under standard conditions.
6-Bromo-4-chloropyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The bromo and chloro substituents offer orthogonal functionalization potential, facilitating sequential derivatization. Its stability under standard reaction conditions and compatibility with diverse coupling partners make it ideal for constructing complex heterocyclic scaffolds 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: