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Structure of 54030-56-7
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6-Amino-3-methyl-2-(methylthio)pyrimidin-4(3H)-one features a uniquely functionalized pyrimidinone core with amino, methyl, and methylthio substituents that enable direct incorporation into bioactive heterocycles. This bench-stable scaffold supports efficient derivatization in medicinal chemistry and materials synthesis.
6-Amino-3-methyl-2-(methylthio)pyrimidin-4(3H)-one serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds relevant to medicinal chemistry. Its amino and methylthio groups offer orthogonal reactivity for functionalization, while the enaminone tautomer stabilizes the core structure under standard reaction conditions. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for scalable synthesis and derivatization in API 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 : H319
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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: