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Structure of 952582-08-0
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4-(6-Bromopyridin-3-yl)morpholine features a brominated pyridine moiety linked to a morpholine ring, delivering a versatile scaffold for medicinal chemistry. The electron-rich morpholine enhances solubility and metabolic stability, while the bromine serves as a pivotal handle for palladium-catalyzed cross-coupling reactions. This compound integrates seamlessly into diverse synthetic pathways requiring targeted functionalization.
4-(6-Bromopyridin-3-yl)morpholine serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. The bromopyridine moiety provides high reactivity in Suzuki, Stille, and Negishi couplings, while the morpholine ring offers favorable solubility and metabolic stability. Bench-stable and readily purified by flash chromatography, it functions reliably in medicinal chemistry campaigns and process development workflows.
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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: