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Structure of 939793-16-5
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tert-Butyl 3-bromopyrrolidine-1-carboxylate features a brominated pyrrolidine core with a robust tert-butyl carbamate protecting group, enabling stable incorporation into complex molecular architectures. The electrophilic bromide facilitates efficient C–C and C–N bond formation under mild conditions. This bench-stable reagent streamlines access to functionalized heterocycles in medicinal chemistry and synthetic methodology development.
tert-Butyl 3-bromopyrrolidine-1-carboxylate serves as a versatile pyrrolidine building block for medicinal chemistry and process development. The bromide moiety enables efficient late-stage functionalization via palladium-catalyzed cross-coupling, while the tert-butyl carbamate group offers excellent stability and convenient deprotection under mild acidic conditions. Its compatibility with diverse reaction conditions facilitates rapid access to substituted pyrrolidines in drug discovery campaigns.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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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-H410
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Precautionary Statements : P264-P270-P273-P280-P330-P391-P501
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Lot numbers can be found on the outside label of a product: