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Structure of 294851-95-9
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4-((5-Bromopyridin-2-yl)methyl)morpholine features a brominated pyridine tethered to a morpholine ring, enabling direct incorporation into bioactive scaffolds. The electron-deficient pyridine moiety pairs with the nucleophilic morpholine nitrogen, facilitating coupling reactions under mild conditions. This compound serves as a key building block in medicinal chemistry for targeted protein labeling and kinase inhibitor development.
4-((5-Bromopyridin-2-yl)methyl)morpholine serves as a versatile building block for late-stage functionalization in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions. The bromopyridine moiety provides high reactivity in Suzuki, Stille, and Negishi transformations, while the morpholine ring offers favorable solubility and metabolic stability. Bench-stable and easily purified, it facilitates efficient synthesis of biologically active heterocyclic scaffolds and pharmaceutical intermediates.
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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-H320-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: