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Structure of 73955-55-2
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Methyl 2-methylpyrimidine-4-carboxylate features a pyrimidine core with strategically positioned methyl and ester groups, enabling direct incorporation into heterocyclic scaffolds. This bench-stable reagent facilitates efficient synthesis of bioactive molecules through palladium-catalyzed cross-coupling and functionalization reactions.
Methyl 2-methylpyrimidine-4-carboxylate serves as a versatile building block in medicinal and synthetic chemistry, enabling efficient access to pyrimidine-based scaffolds. Its methyl and ester functionalities offer orthogonal reactivity for further derivatization, including nucleophilic substitution, hydrogenation, and coupling reactions. The compound exhibits good bench stability and is readily purified by standard chromatographic methods, facilitating integration into multi-step synthesis 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 : H302-H315-H320-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: