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Structure of 1227586-61-9
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4-Fluoro-3-methylpyridin-2-amine features a strategically positioned fluorine atom and methyl group on the pyridine ring, enabling enhanced electronic modulation and metabolic stability. This electron-deficient heterocycle integrates readily into pharmaceutical scaffolds, serving as a key building block for kinase inhibitors and CNS-targeted therapeutics.
4-Fluoro-3-methylpyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds through palladium-catalyzed cross-coupling reactions. Its fluorine and amino groups provide orthogonal reactivity for late-stage functionalization, while the methyl substituent enhances metabolic stability. The compound exhibits excellent bench stability and is compatible with standard purification protocols, facilitating integration into multi-step synthesis 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: