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Structure of 569660-97-5
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tert-Butyl (R)-3-bromopyrrolidine-1-carboxylate is a chiral building block featuring a stereodefined bromide at the 3-position of a pyrrolidine ring. This bench-stable, moisture-tolerant reagent facilitates asymmetric synthesis through selective C–X bond formation. The tert-butyl carbamate group enables convenient protection and deprotection, streamlining access to complex nitrogen-containing scaffolds in medicinal chemistry and peptide analog development.
tert-Butyl (R)-3-bromopyrrolidine-1-carboxylate serves as a stereochemically defined building block for the synthesis of bioactive pyrrolidine-containing molecules. The bromide functionality enables efficient late-stage functionalization via palladium-catalyzed cross-coupling, while the tert-butyl carbamate group provides excellent stability and ease of removal under mild acidic conditions. Its configurational integrity and compatibility with diverse reaction conditions make it a practical choice for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS08,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H319-H372-H400
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Precautionary Statements : P280-P373-P501
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Lot numbers can be found on the outside label of a product: