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Structure of 1369814-75-4
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tert-Butyl (16-bromohexadecyl)carbamate features a long hydrophobic alkyl chain terminated by a bromo group and a stable carbamate protecting group. This bifunctional reagent enables site-specific conjugation in peptide synthesis and surface functionalization, combining efficient coupling chemistry with excellent stability under standard conditions.
tert-Butyl (16-bromohexadecyl)carbamate serves as a robust, bench-stable protecting group for primary amines in long-chain alkylamine synthesis. Its bromide functionality enables efficient post-functionalization via palladium-catalyzed cross-coupling, facilitating the construction of complex alkylated scaffolds. The tert-butyl carbamate moiety ensures high stability under diverse reaction conditions and simplifies purification through straightforward acidolysis. This reagent is particularly valuable in the synthesis of lipid-conjugated molecules and membrane-targeted pharmaceutical intermediates.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: