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Structure of 13509-52-9
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1,3,6-Trimethylpyrimidine-2,4(1H,3H)-dione features a sterically hindered pyrimidine core with methyl groups at key positions, enhancing stability and modulating reactivity. This scaffold serves as a robust building block in medicinal chemistry, enabling efficient access to bioactive heterocycles through selective functionalization.
1,3,6-Trimethylpyrimidine-2,4(1H,3H)-dione serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrimidinediones through standard alkylation and condensation protocols. Its three methyl groups enhance solubility and facilitate purification, while the diketone functionality supports diverse transformations including nucleophilic addition and cyclization. The compound exhibits excellent bench stability and functional group tolerance, making it well-suited for iterative synthesis 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: