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Structure of 139626-20-3
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2-Chloro-4-fluoro-5-nitroaniline features a trifunctional aromatic core with electron-withdrawing halogens and a nitro group, enabling precise coupling in pharmaceutical intermediates. This bench-stable derivative integrates readily into complex scaffolds under standard conditions.
2-Chloro-4-fluoro-5-nitroaniline serves as a key intermediate in the synthesis of bioactive heterocycles and pharmaceutical scaffolds. Its electron-deficient aromatic core enables efficient coupling reactions, while the orthogonal reactivity of the chloro, fluoro, and nitro groups facilitates sequential functionalization. Bench-stable and compatible with standard purification methods, it functions effectively in cross-coupling, nucleophilic substitution, and reduction protocols essential to medicinal chemistry workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: