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Structure of 1506878-13-2
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This dihydropyrimidinone features a 4-bromo-2,6-dimethylphenyl group fused to a pyrimidine core, delivering enhanced stability and tunable reactivity. The electron-deficient bromine substituent enables efficient cross-coupling transformations, while the bench-stable scaffold integrates readily into medicinal chemistry campaigns requiring modular heterocyclic platforms.
1-(4-Bromo-2,6-dimethylphenyl)dihydropyrimidine-2,4(1H,3H)-dione serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds. The bromo group facilitates palladium-catalyzed cross-coupling reactions, while the dihydropyrimidinone core exhibits excellent bench stability and compatibility with diverse functional groups. Its structure supports modular synthesis of bioactive molecules and provides a robust platform for late-stage diversification in drug discovery workflows.
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Lot numbers can be found on the outside label of a product: