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Structure of 1979-98-2
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2-Methylthio-4,6-pyrimidinedione features a thioether-functionalized pyrimidine core with enhanced stability and solubility in polar solvents. This scaffold serves as a key intermediate in the synthesis of nucleoside analogs and heterocyclic pharmaceuticals, offering predictable reactivity at C4 and C6 positions.
2-Methylthio-4,6-pyrimidinedione serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds through nucleophilic substitution and condensation reactions. Its methylthio group facilitates selective functionalization, while the diketone framework supports robust reactivity in standard synthetic workflows. The compound exhibits good bench stability and is amenable to purification via recrystallization, making it well-suited for industrial R&D and medicinal chemistry applications.
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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: