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Structure of 1261988-16-2
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5-Bromo-1,2-difluoro-3-nitrobenzene features a trifunctional aromatic core with orthogonal reactivity, enabling selective coupling in late-stage functionalization. The electron-deficient ring facilitates nucleophilic substitution, while the bromo and difluoro groups offer complementary handles for cross-coupling and fluorination processes. This compound serves as a key intermediate in the synthesis of bioactive molecules and advanced materials.
5-Bromo-1,2-difluoro-3-nitrobenzene serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined halogen reactivity. The ortho-fluoro substitution enhances metabolic stability, while the nitro group provides a handle for selective reduction or further functionalization. Bench-stable and readily purified, it facilitates efficient access to complex heterocyclic scaffolds and substituted aromatic systems in multi-step syntheses.
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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: