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Structure of 407-22-7
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2-Fluoro-6-methylpyridine serves as a key heterocyclic building block in medicinal chemistry, featuring a fluorinated ring and a methyl substituent that enhance metabolic stability and modulate electronic properties. This bench-stable, moisture-tolerant scaffold integrates readily into diverse synthetic pathways, enabling efficient access to bioactive compounds with tailored pharmacokinetic profiles.
2-Fluoro-6-methylpyridine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the pyridine ring via palladium-catalyzed cross-coupling. Its fluorine and methyl groups provide orthogonal reactivity and enhanced metabolic stability, while its bench-stable nature facilitates handling and purification. Functions as a key scaffold for kinase inhibitors and CNS-targeted therapeutics.
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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 : H227-H315-H319-H335
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Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: