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Structure of 914347-01-6
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Methyl 1-(5-bromopyrimidin-2-yl)piperidine-4-carboxylate features a brominated pyrimidine moiety linked to a piperidine scaffold, enabling direct integration into diverse synthetic pathways. The ester group offers tunable reactivity, while the electron-deficient heterocycle facilitates cross-coupling and nucleophilic substitution reactions under standard conditions. This compound serves as a key building block for functionalized pharmaceutical intermediates.
Methyl 1-(5-bromopyrimidin-2-yl)piperidine-4-carboxylate serves as a versatile building block for the synthesis of pyrimidine-containing heterocycles, enabling efficient Suzuki-Miyaura and Buchwald-Hartwig coupling reactions. The bromopyrimidine moiety offers high reactivity in palladium-catalyzed transformations, while the piperidine carboxylate functionality provides excellent functional group tolerance and stability under standard reaction conditions. This compound facilitates rapid access to biologically relevant scaffolds used in medicinal chemistry and process development.
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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-H332-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: