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Structure of 136227-39-9
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Methyl 2-bromo-5-methylnicotinate is a brominated nicotinate ester featuring a methyl group at the 5-position and a bromine atom at the 2-position. This electron-deficient heterocycle integrates readily into cross-coupling reactions, offering enhanced reactivity in palladium-catalyzed transformations. The ester functionality enables straightforward derivatization, while the steric profile of the 5-methyl substituent improves stability under standard reaction conditions.
Methyl 2-bromo-5-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 further derivatization, while the pyridine core offers inherent stability and compatibility with standard reaction conditions. This compound facilitates efficient access to substituted nicotinates and related pharmaceutical scaffolds.
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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-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: