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Structure of 1627-27-6
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1,6-Dimethylpyrimidine-2,4(1H,3H)-dione features a symmetric diketone core with methyl substituents at the 1 and 6 positions, enhancing stability and solubility in polar solvents. This scaffold serves as a key building block in heterocyclic synthesis, particularly for pyrimidine-based pharmaceutical intermediates. The molecule exhibits robust bench stability under standard conditions, facilitating straightforward handling in synthetic workflows.
1,6-Dimethylpyrimidine-2,4(1H,3H)-dione serves as a stable, bench-ready building block for heterocyclic synthesis. Its dimethyl-substituted pyrimidinedione core exhibits predictable reactivity in nucleophilic substitution and condensation reactions, enabling efficient access to functionalized pyrimidine scaffolds. The molecule demonstrates excellent solubility in common organic solvents and tolerates a range of functional groups, facilitating straightforward purification and integration into multi-step synthetic sequences.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362+P364
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Lot numbers can be found on the outside label of a product: