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Structure of 211315-53-6
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tert-Butyl (R)-(2-(4-bromophenyl)propyl)carbamate features a chiral benzylic center with a brominated phenyl group, delivering high stereochemical fidelity. This bench-stable carbamate serves as a protected amine handle in asymmetric synthesis, enabling selective coupling and functionalization under standard conditions.
tert-Butyl (R)-(2-(4-bromophenyl)propyl)carbamate serves as a stable, bench-ready chiral building block for asymmetric synthesis. The carbamate group enables mild deprotection under acidic conditions, while the pendant 4-bromophenyl moiety supports palladium-catalyzed cross-coupling reactions. Its stereochemical integrity and functional group tolerance make it ideal for constructing biologically relevant scaffolds in medicinal chemistry and process development 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 : 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: