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Structure of 1194-21-4
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2-Amino-6-chloropyrimidin-4(3H)-one features a fused heterocyclic core with amino and chloro substituents enabling versatile functionalization. This bench-stable compound integrates readily into pharmaceutical scaffolds, offering enhanced solubility and metabolic stability in bioactive molecule design.
2-Amino-6-chloropyrimidin-4(3H)-one serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its amino and chloro substituents facilitate nucleophilic substitution and transition-metal-catalyzed coupling reactions, while the enolizable carbonyl supports condensation and cyclization processes. The compound exhibits good bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis campaigns targeting kinase inhibitors and antiviral agents.
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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: