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Structure of 98612-60-3
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(R)-5-(Bromomethyl)pyrrolidin-2-one features a stereodefined pyrrolidinone core with a reactive bromomethyl handle at the 5-position. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences requiring selective alkylation or chain extension. The chiral scaffold supports asymmetric synthesis and enables access to complex nitrogen-containing architectures.
(R)-5-(Bromomethyl)pyrrolidin-2-one serves as a versatile chiral building block for the synthesis of bioactive heterocycles and medicinal chemistry intermediates. The bromomethyl group enables efficient nucleophilic substitution, while the pyrrolidinone scaffold offers excellent functional group tolerance and bench stability. Its stereochemical integrity supports reliable incorporation into complex molecular architectures via standard coupling protocols.
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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-H317-H319
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: