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Structure of 305329-97-9
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tert-Butyl 3-(bromomethyl)pyrrolidine-1-carboxylate features a bromomethyl group attached to a pyrrolidine ring, enabling direct functionalization in late-stage synthesis. The tert-butyl ester provides stability and ease of deprotection under mild acidic conditions. This reagent integrates readily into diversification workflows for medicinal chemistry and peptide modification.
tert-Butyl 3-(bromomethyl)pyrrolidine-1-carboxylate serves as a versatile building block for the synthesis of pyrrolidine-based scaffolds, enabling efficient introduction of bromomethyl functionality at the 3-position. Its bench-stable nature and compatibility with palladium-catalyzed cross-coupling reactions facilitate rapid diversification in medicinal chemistry campaigns. The tert-butyl carbamate group provides orthogonal protection and can be readily removed under mild acidic conditions.
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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#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302+H312-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P302+P352-P304+P340-P330-P362+P364-P363-P405-P501
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Lot numbers can be found on the outside label of a product: