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Structure of 1067230-64-1
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(S)-1-Boc-3-(Bromomethyl)pyrrolidine features a stereodefined pyrrolidine core with a Boc-protected amine and a bromomethyl group at the 3-position. This bifunctional building block enables site-selective coupling reactions, integrating readily into peptide extensions or complex heterocycles. The pendant bromide serves as a potent electrophile for nucleophilic substitution, while the Boc group ensures stability during manipulations. Its bench-stable nature supports straightforward handling in synthetic workflows.
(S)-1-Boc-3-(Bromomethyl)pyrrolidine serves as a versatile chiral building block for the synthesis of pyrrolidine-containing pharmaceuticals and bioactive molecules. The bromomethyl group enables efficient alkylation and Suzuki-type coupling reactions, while the Boc-protected amine ensures stability and compatibility with standard synthetic workflows. Its stereochemical integrity facilitates enantioselective transformations, making it ideal for medicinal chemistry applications requiring precise stereocontrol.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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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: