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Structure of 15931-21-2
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3-Fluoro-2-methylpyridin-4-amine features a strategically positioned fluorine atom and methyl group on the pyridine ring, enhancing electronic modulation and metabolic stability. This electron-deficient heterocycle serves as a key scaffold in kinase inhibitor design and medicinal chemistry optimization.
3-Fluoro-2-methylpyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds through standard coupling reactions. Its fluorinated heterocyclic core offers enhanced metabolic stability and favorable pharmacokinetic properties, while the ortho-methyl and amine groups provide orthogonal reactivity for further functionalization. The compound exhibits good bench stability and is compatible with common synthetic transformations, facilitating rapid diversification in drug discovery campaigns.
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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-H319
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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: