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Structure of 89379-73-7
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2-Oxo-3H-pyrimidine-4-carboxylic acid features a conjugated pyrimidinone core with a carboxylic acid at the C4 position, enabling direct integration into heterocyclic scaffolds. The electron-deficient ring system facilitates nucleophilic substitution and coupling reactions under mild conditions. This bench-stable compound serves as a key building block in medicinal chemistry for synthesizing kinase inhibitors and antiviral agents.
2-Oxo-3H-pyrimidine-4-carboxylic acid serves as a versatile building block for pyrimidine-based heterocycles, enabling efficient access to pharmaceutically relevant scaffolds. Its carboxylic acid functionality facilitates direct derivatization and coupling reactions, while the 2-oxo group supports further functionalization via nucleophilic addition or condensation pathways. The compound exhibits good bench stability and is compatible with standard synthetic workflows, making it suitable for medicinal chemistry campaigns requiring rapid analog generation.
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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: