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Structure of 1391026-59-7
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tert-Butyl (1-bromopropan-2-yl)carbamate features a brominated chiral center flanked by a stable tert-butyl carbamate group, enabling direct functionalization in late-stage synthesis. This bench-stable reagent integrates seamlessly into iterative coupling workflows, offering reliable access to complex amine derivatives under standard conditions.
tert-Butyl (1-bromopropan-2-yl)carbamate serves as a stable, bench-ready carbamate protecting group for primary amines, enabling selective N-alkylation and subsequent deprotection under mild acidic conditions. Its bromo substituent provides a versatile handle for further functionalization via palladium-catalyzed cross-coupling reactions. The compound exhibits excellent functional group tolerance and facilitates efficient synthesis of complex amine-containing intermediates 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 : H302
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Precautionary Statements : P264-P270-P301+P310-P330-P501
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Lot numbers can be found on the outside label of a product: