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Structure of 2369-19-9
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2-Fluoro-5-methylpyridine serves as a key heterocyclic building block in medicinal chemistry, featuring a fluorine atom at the 2-position and a methyl group at the 5-position on the pyridine ring. This electronic and steric profile enhances metabolic stability and modulates bioavailability, making it valuable for drug discovery applications.
2-Fluoro-5-methylpyridine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the pyridine ring via palladium-catalyzed cross-coupling reactions. Its fluorine and methyl substituents provide orthogonal reactivity and enhanced metabolic stability, while its bench-stable nature facilitates handling and purification in multi-step syntheses.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H315-H319-H335
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: