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Structure of 828272-19-1
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tert-Butyl (3-bromopropyl)(methyl)carbamate features a bromoalkyl handle flanked by a methyl-substituted carbamate and sterically shielded tert-butyl group, enabling selective conjugation under mild conditions. This bench-stable reagent integrates readily into bioconjugation workflows, delivering controlled functionalization of nucleophiles without catalyst dependency.
tert-Butyl (3-bromopropyl)(methyl)carbamate serves as a versatile bifunctional building block, enabling efficient introduction of both a bromoalkyl chain and a protected amine moiety in synthetic sequences. The tert-butyl carbamate group provides excellent stability under basic conditions and facilitates straightforward deprotection via mild acidolysis. Its reactivity profile supports reliable alkylation reactions and incorporation into heterocyclic scaffolds, making it a practical choice for medicinal chemistry and process-scale synthesis 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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: