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Structure of 1415841-82-5
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tert-Butyl 5-bromo-1,2,3,6-tetrahydropyridine-1-carboxylate features a brominated tetrahydropyridine core with a bench-stable tert-butyl ester handle. This electrophilic scaffold enables direct coupling in cross-coupling reactions and facilitates downstream functionalization in medicinal chemistry. The electron-deficient pyridine ring enhances reactivity in palladium-catalyzed transformations.
tert-Butyl 5-bromo-1,2,3,6-tetrahydropyridine-1-carboxylate serves as a versatile building block for the synthesis of substituted pyridine derivatives. The bromine at C5 enables palladium-catalyzed cross-coupling reactions, while the protected tetrahydropyridine core offers controlled reactivity in functional group interconversions. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient access to complex heterocyclic scaffolds relevant to medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-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: