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Structure of 1393574-54-3
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5-Chloro-4-fluoropyridin-2-amine features a strategically positioned chloro and fluoro substituent on the pyridine ring, enabling selective coupling reactions in medicinal chemistry. The electron-deficient heterocycle integrates readily into kinase inhibitors and bioactive scaffolds, offering enhanced metabolic stability and favorable binding affinity. This bench-stable reagent supports efficient transition metal-catalyzed transformations under standard conditions.
5-Chloro-4-fluoropyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated heterocyclic scaffolds. Its orthogonal reactivity—where the amine group facilitates nucleophilic substitution and the halogens support palladium-catalyzed coupling—enables modular synthesis of complex APIs. Bench-stable and readily purified, it functions effectively in standard cross-coupling, cyclization, and derivatization workflows common in drug discovery.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: