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Structure of 1067230-65-2
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(R)-1-Boc-3-(Bromomethyl)pyrrolidine features a stereodefined pyrrolidine core with a Boc-protected amine and a pendant bromomethyl group. This bifunctional handle enables selective alkylation or transition-metal-catalyzed coupling reactions in synthetic organic chemistry, particularly in the construction of nitrogen-containing heterocycles and bioactive molecules. The Boc group ensures stability under basic conditions while the bromide offers high reactivity for nucleophilic substitution.
(R)-1-Boc-3-(Bromomethyl)pyrrolidine serves as a versatile chiral building block for the synthesis of bioactive heterocycles and peptidomimetics. The bromomethyl group enables efficient nucleophilic substitution, while the Boc-protected amine offers orthogonal handling in multi-step sequences. Its bench-stable nature and compatibility with standard coupling conditions facilitate streamlined access to complex scaffolds in medicinal chemistry and process development.
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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: