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Structure of 327046-79-7
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tert-Butyl (4-bromo-2-nitrophenyl)carbamate features a bromo-substituted nitroaryl scaffold with a bench-stable carbamate protecting group. This reagent enables direct functionalization at the para position while maintaining compatibility with palladium-catalyzed cross-coupling reactions. The electron-deficient aromatic ring enhances regioselective transformation, and the tert-butyl carbamate delivers predictable deprotection under mild acidic conditions.
tert-Butyl (4-bromo-2-nitrophenyl)carbamate serves as a versatile building block in medicinal chemistry, enabling the selective introduction of bromo- and nitro-functionalized aryl intermediates. The carbamate group provides excellent bench stability and facilitates orthogonal protection during multi-step synthesis. It readily participates in palladium-catalyzed cross-coupling reactions and undergoes controlled reduction to access amino-substituted scaffolds. Its compatibility with standard purification protocols and functional group tolerance make it well-suited for scalable API intermediate development.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: