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Structure of 301221-79-4
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tert-Butyl 4-(2-bromoacetyl)piperidine-1-carboxylate features a bromoacetyl group attached to a piperidine scaffold, enabling direct functionalization in synthetic sequences. This bench-stable reagent facilitates efficient C–C and C–heteroatom bond formation via nucleophilic substitution, particularly valuable in peptide derivatization and medicinal chemistry applications.
tert-Butyl 4-(2-bromoacetyl)piperidine-1-carboxylate serves as a versatile building block for the synthesis of piperidine-containing scaffolds, enabling efficient introduction of a bromoacetyl group at the nitrogen. Its bench-stable nature and compatibility with standard coupling reactions facilitate downstream functionalization, including nucleophilic substitution and heterocycle formation. The tert-butyl carbamate group provides orthogonal protection, allowing selective transformations in complex molecule assembly.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: