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Structure of 405230-90-2
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2-Chloro-5-fluoro-3-nitropyridin-4-amine features a pyridine core functionalized with chlorine, fluorine, nitro, and amino groups at strategic positions. This electron-deficient heterocycle serves as a high-impact scaffold for constructing advanced pharmaceutical intermediates, leveraging its reactivity in cross-coupling and nucleophilic substitution processes under standard conditions.
2-Chloro-5-fluoro-3-nitropyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling the construction of nitrogen-containing heterocycles via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. Its orthogonal reactivity—combining a chloro group for Suzuki-Miyaura coupling, a fluoro group for site-selective displacement, and a nitro group amenable to reduction—facilitates efficient diversification. Bench-stable and readily purified by recrystallization, it functions as a key intermediate in the synthesis of kinase inhibitors and other bioactive scaffolds.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: