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Structure of 16952-65-1
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Pyrido[4,3-d]pyrimidine-2,4(1H,3H)-dione delivers a rigid, electron-deficient heterocyclic scaffold ideal for medicinal chemistry. This fused bicyclic core integrates hydrogen-bonding capacity and planar geometry, enabling strong interactions in target binding. Bench-stable and compatible with standard synthetic protocols, it serves as a strategic building block for kinase inhibitors and nucleoside analogs.
Pyrido[4,3-d]pyrimidine-2,4(1H,3H)-dione serves as a versatile heterocyclic scaffold in medicinal chemistry, enabling efficient access to fused pyridopyrimidinone frameworks. Its diketone functionality facilitates nucleophilic addition and condensation reactions, supporting derivatization at multiple sites. The compound exhibits good bench stability and is compatible with standard purification methods, making it a practical building block for targeted synthesis of kinase inhibitors and other bioactive molecules.
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Lot numbers can be found on the outside label of a product: