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Structure of 172846-33-2
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1,3-Bis(1,1-dimethylethyl)-2-(3-bromopropyl)imidodicarbonate features a sterically shielded imidodicarbonate core paired with a reactive bromopropyl handle. This bench-stable reagent enables efficient coupling in synthetic workflows, particularly for introducing protected carbamate functionalities under mild conditions.
1,3-Bis(1,1-dimethylethyl)-2-(3-bromopropyl)imidodicarbonate serves as a robust, bench-stable building block for the synthesis of functionalized heterocycles and protected amino acid derivatives. Its bromopropyl side chain enables efficient coupling reactions via nucleophilic substitution, while the imidodicarbonate moiety provides orthogonal protection compatible with standard deprotection protocols. The tert-butyl groups confer enhanced stability and ease of purification, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS06,GHS08
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Signal Word : Danger
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UN#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331-H341
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P361-P405-P501
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Lot numbers can be found on the outside label of a product: