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Structure of 446-09-3
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1-Bromo-4-fluoro-2-nitrobenzene features a trifunctional aryl scaffold enabling sequential cross-coupling and nucleophilic substitution. The electron-deficient ring enhances reactivity in palladium-catalyzed processes, while the bromo and fluoro groups offer orthogonal functionalization handles. This bench-stable compound integrates seamlessly into complex molecule assembly workflows.
1-Bromo-4-fluoro-2-nitrobenzene serves as a versatile building block in cross-coupling and nucleophilic aromatic substitution reactions. The ortho-difunctionalized aryl scaffold enables sequential functionalization, with the bromide facilitating palladium-catalyzed couplings and the fluoride enabling selective displacement under mild conditions. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for constructing complex heterocycles and pharmaceutical intermediates.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302+H312-H315-H319-H331-H335
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: