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Structure of 1328360-41-3
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N-(6-bromopyridin-3-yl)methanesulfonamide features a brominated pyridine core paired with a sulfonamide handle, enabling direct incorporation into Suzuki-Miyaura cross-coupling reactions. This bench-stable reagent delivers efficient access to functionalized heterocycles under standard conditions.
N-(6-Bromopyridin-3-yl)methanesulfonamide serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromopyridine moiety provides high reactivity in Suzuki, Stille, and Negishi couplings, while the methanesulfonamide group offers excellent solubility and metabolic stability. Bench-stable and readily purified by flash chromatography, it functions as a key intermediate in the synthesis of kinase inhibitors and other bioactive heterocycles.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: