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Structure of 3137-60-8
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5-Amino-6-chloro-1H-pyrimidin-4-one features a fused heterocyclic core with complementary amino and chloro substituents, enabling direct functionalization in medicinal chemistry. This electron-deficient pyrimidinone integrates readily into bioactive scaffolds under standard conditions, offering high reactivity and stability for synthetic applications.
5-Amino-6-chloro-1H-pyrimidin-4-one serves as a versatile building block in medicinal chemistry, enabling the synthesis of pyrimidine-based scaffolds through nucleophilic substitution and coupling reactions. The amino group facilitates derivatization, while the chloro substituent provides a reliable handle for palladium-catalyzed cross-coupling. Its bench-stable crystalline form and compatibility with standard purification methods make it well-suited for high-throughput synthesis and process development.
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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: