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Structure of 128412-15-7
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tert-Butyl (4-bromobutan-2-yl)carbamate delivers a bifunctional handle combining a stable carbamate protecting group with a reactive bromide for downstream coupling. This bench-stable reagent facilitates efficient incorporation into complex scaffolds via nucleophilic substitution, enabling streamlined synthesis of functionalized intermediates in medicinal chemistry and peptide derivatization workflows.
tert-Butyl (4-bromobutan-2-yl)carbamate serves as a versatile bifunctional building block in synthetic organic chemistry, combining a stable tert-butyl carbamate (Boc) protecting group with a pendant bromide for downstream functionalization. The bromide enables palladium-catalyzed cross-coupling reactions, while the Boc group provides orthogonal protection compatible with standard deprotection protocols. Its bench-stable nature and ease of purification make it well-suited for iterative synthesis of complex molecules, including pharmaceutical intermediates and heterocyclic scaffolds.
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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-P330
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Lot numbers can be found on the outside label of a product: