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Structure of 1075705-01-9
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4-Fluoro-2-methoxy-5-nitroaniline features a trifunctional aromatic core combining electron-withdrawing nitro and fluoro groups with a methoxy donor, enabling tailored reactivity in cross-coupling and heterocycle synthesis. This bench-stable derivative integrates readily into complex molecular architectures under standard conditions.
4-Fluoro-2-methoxy-5-nitroaniline serves as a versatile building block in the synthesis of pharmaceutical intermediates and agrochemicals. Its electron-deficient aromatic core, combined with orthogonal functional groups—fluorine for metabolic stability, methoxy for synthetic handle, and nitro for reduction to amine—enables diverse transformations. The compound exhibits bench stability and facilitates efficient coupling reactions, making it well-suited for multi-step syntheses requiring selective reactivity and predictable transformation pathways.
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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: