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Structure of 94133-62-7
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4-Amino-3,5-dichloro-6-fluoropyridin-2(1H)-one features a highly electron-deficient pyridinone core with orthogonal functional groups enabling direct incorporation into pharmaceutical scaffolds. The amino group supports facile derivatization, while the dichloro and fluoro substituents enhance metabolic stability and modulate electronic properties. This compound serves as a key intermediate in the synthesis of kinase inhibitors and bioactive heterocycles.
4-Amino-3,5-dichloro-6-fluoropyridin-2(1H)-one serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pyridone-based scaffolds. Its complementary electron-withdrawing substituents facilitate nucleophilic substitution and transition-metal-catalyzed coupling reactions. The molecule exhibits bench stability, moderate solubility, and compatibility with standard purification methods, making it well-suited for medicinal chemistry 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: