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Structure of 54376-50-0
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5-Fluoro-2-methylpyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, offering enhanced metabolic stability and targeted electronic properties. This bench-stable compound integrates readily into kinase inhibitors and antiviral agents, where its electron-deficient ring system facilitates selective binding interactions.
5-Fluoro-2-methylpyrimidine serves as a versatile building block in medicinal chemistry, enabling direct C–H functionalization and transition-metal-catalyzed cross-coupling reactions. Its electron-deficient pyrimidine core exhibits enhanced reactivity at C5 due to the fluorine substituent, while the 2-methyl group provides steric and electronic modulation. The compound demonstrates excellent bench stability and compatibility with diverse reaction conditions, facilitating efficient incorporation into heterocyclic scaffolds and API intermediates.
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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: