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Structure of 1256276-41-1
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6-Bromo-5-fluoropyridin-3-amine features a halogenated pyridine core with complementary bromo and fluoro substituents at adjacent positions, enabling selective functionalization in cross-coupling reactions. The amino group at C3 provides a reactive handle for derivatization, while the electron-withdrawing halogens enhance electrophilicity. This combination supports efficient diversification in medicinal chemistry and materials synthesis under standard conditions.
6-Bromo-5-fluoropyridin-3-amine serves as a versatile building block for the synthesis of bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions due to its reactive halogen and amine functionalities. The ortho-bromofluoro substitution pattern provides excellent regiocontrol in Suzuki, Buchwald–Hartwig, and other transition-metal-mediated transformations. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for iterative medicinal chemistry campaigns and API intermediate 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: