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Structure of 6153-44-2
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Methyl 2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylate features a uniquely reactive pyrimidine core with adjacent carbonyl and ester functionalities. This bench-stable heterocycle integrates readily into multicomponent condensations, serving as a versatile synthon for nitrogen-rich scaffolds in medicinal chemistry and materials synthesis.
Methyl 2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine cores via standard condensation and cyclization protocols. Its dual carbonyl and ester functionalities offer orthogonal reactivity for functional group manipulation, while its bench stability and straightforward purification support reliable use in 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 : 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: