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Structure of 1382847-91-7
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Methyl 5-bromo-4-methylnicotinate is a bench-stable, electron-deficient heterocyclic ester featuring a bromine atom at the C5 position and a methyl group at C4. This configuration enables direct functionalization in palladium-catalyzed cross-coupling reactions, streamlining access to substituted nicotinates for medicinal chemistry and materials synthesis.
Methyl 5-bromo-4-methylnicotinate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine functionality. The methyl ester and methyl substituent provide orthogonal handles for selective transformations, while the pyridine core offers stability and compatibility with standard reaction conditions. Its bench-stable nature and predictable reactivity make it ideal for constructing complex scaffolds in medicinal chemistry and materials science applications.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: