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Structure of 16462-28-5
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6-Amino-2-oxo-1,2-dihydropyrimidine-5-carbonitrile features a fused heterocyclic core bearing an amino group at C6 and a nitrile function at C5, enabling direct incorporation into bioactive scaffolds. The electron-deficient pyrimidinone ring facilitates nucleophilic addition and transition-metal-catalyzed coupling reactions. This bench-stable, moisture-tolerant compound serves as a key building block for pharmaceutical intermediates and functional materials.
6-Amino-2-oxo-1,2-dihydropyrimidine-5-carbonitrile serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds. Its amino and nitrile functionalities support diverse transformations, including cyclizations, amidations, and metal-catalyzed couplings. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative medicinal chemistry campaigns and process development 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: