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Structure of 1805069-44-6
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3-Fluoro-2-methyl-6-nitropyridine features a strategically positioned fluorine atom and electron-deficient nitro group, enabling selective functionalization in cross-coupling reactions. The methyl substituent enhances regiocontrol, while the pyridine core provides robust stability under standard conditions. This compound serves as a key building block for bioactive heterocycles and advanced pharmaceutical intermediates.
3-Fluoro-2-methyl-6-nitropyridine serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling. The ortho-fluoro and nitro groups facilitate selective C–H activation and nucleophilic substitution, while the methyl group provides steric and electronic modulation. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for iterative synthesis of heterocyclic scaffolds relevant to pharmaceutical 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: