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Structure of 5571-03-9
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Methyl 2-methylpyrimidine-5-carboxylate is a bench-stable pyrimidine derivative featuring a methyl group at the 2-position and a carboxylate ester at the 5-position. This configuration imparts enhanced solubility in organic solvents and facilitates direct incorporation into heterocyclic scaffolds via cross-coupling or nucleophilic substitution reactions, streamlining access to bioactive intermediates in medicinal chemistry.
Methyl 2-methylpyrimidine-5-carboxylate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to pyrimidine-based scaffolds. Its methyl ester group facilitates straightforward derivatization, while the 2-methyl substitution enhances regioselectivity in downstream functionalizations. The compound exhibits good bench stability and compatibility with standard coupling and cyclization protocols, making it suitable for modular synthesis of bioactive heterocycles.
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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-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: