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Structure of 1227562-32-4
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Methyl 6-bromo-2-methylnicotinate is a brominated nicotinate ester featuring a methyl group at the 2-position and a bromine atom at the 6-position of the pyridine ring. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, enabling efficient coupling reactions for the synthesis of functionalized pharmaceutical intermediates. The molecule exhibits enhanced reactivity in cross-coupling transformations due to the ortho-directing effect of the methyl group and the strong electron-withdrawing nature of the bromide. Its bench-stable solid form facilitates handling under standard laboratory conditions.
Methyl 6-bromo-2-methylnicotinate serves as a versatile building block for the synthesis of substituted nicotinates and heterocyclic scaffolds. The bromine at the 6-position enables palladium-catalyzed cross-coupling reactions, while the methyl group at C2 enhances regioselectivity in electrophilic functionalization. Its bench-stable nature and compatibility with standard purification protocols facilitate efficient integration into medicinal chemistry 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: