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Structure of 84476-99-3
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2,5-Difluoropyridine serves as a key heterocyclic scaffold in medicinal chemistry, offering enhanced metabolic stability and modulated electron density. The strategically positioned fluorine atoms enable directed functionalization via cross-coupling reactions, while the electron-deficient core facilitates nucleophilic substitution. This bench-stable, moisture-tolerant reagent integrates efficiently into complex molecular architectures.
2,5-Difluoropyridine serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling site-selective functionalization via cross-coupling and nucleophilic substitution reactions. Its orthogonal reactivity profile, enhanced by the electron-withdrawing effect of fluorine atoms, facilitates efficient C–H activation and late-stage diversification. Bench-stable and compatible with standard reaction conditions, it functions as a key scaffold for heterocyclic API development and catalyst design.
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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-P302+P352
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Lot numbers can be found on the outside label of a product: