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Structure of 1261584-19-3
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5-Bromo-2-methoxypyridine-3-sulfonyl chloride features a reactive sulfonyl chloride group flanked by electron-withdrawing bromo and methoxy substituents, enabling selective acylation in heterocyclic synthesis. This bench-stable reagent integrates efficiently into complex molecular architectures under standard conditions, delivering high functional group tolerance and clean reaction profiles for advanced intermediates in medicinal chemistry and materials science applications.
5-Bromo-2-methoxypyridine-3-sulfonyl chloride serves as a versatile building block for sulfonamide synthesis, enabling efficient incorporation of a brominated pyridyl sulfonamide motif into target molecules. The reagent exhibits excellent bench stability and facilitates direct coupling with amines under mild conditions, offering high functional group tolerance and straightforward purification. Its reactivity profile supports applications in medicinal chemistry and process development, particularly in the construction 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: