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Structure of 181258-46-8
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tert-Butyl 2-(bromomethyl)pyrrolidine-1-carboxylate features a bromomethyl group attached to a pyrrolidine ring, enabling efficient alkylation reactions. The tert-butyl ester moiety provides stability and ease of removal under mild acidic conditions. This reagent integrates readily into complex molecular architectures, particularly in medicinal chemistry and peptide derivatization workflows.
tert-Butyl 2-(bromomethyl)pyrrolidine-1-carboxylate serves as a versatile building block for the synthesis of pyrrolidine-based scaffolds in medicinal chemistry. The bromomethyl group enables efficient nucleophilic substitution reactions, facilitating the installation of diverse functional groups. Its tert-butyl carbamate protection offers excellent bench stability and compatibility with standard coupling protocols, enabling straightforward purification and broad utility in peptide and heterocyclic compound synthesis.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1760
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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 : 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: