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Structure of 16952-64-0
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Pyrido[4,3-d]pyrimidin-4(3H)-one features a fused heteroaromatic core with hydrogen-bonding capacity at the lactam carbonyl and N-H positions. This scaffold serves as a privileged motif in medicinal chemistry, enabling robust integration into kinase inhibitors and nucleoside analogs due to its planar geometry and favorable binding interactions.
Pyrido[4,3-d]pyrimidin-4(3H)-one serves as a privileged scaffold in medicinal chemistry, enabling efficient access to biologically active heterocycles. Its fused bicyclic structure exhibits robust bench stability and tolerates diverse functional groups, facilitating downstream derivatization via standard coupling, alkylation, and nucleophilic substitution reactions. The core functions effectively in the synthesis of kinase inhibitors and other targeted therapeutics, offering predictable reactivity in established synthetic 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 : 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: