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Structure of 1187932-69-9
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tert-Butyl (R)-3-(iodomethyl)pyrrolidine-1-carboxylate features a chiral pyrrolidine core with a bench-stable, moisture-tolerant tert-butyl ester and a reactive iodomethyl handle. This configuration enables selective alkylation in late-stage functionalization, particularly in the synthesis of bioactive heterocycles and pharmaceutical intermediates.
tert-Butyl (R)-3-(iodomethyl)pyrrolidine-1-carboxylate serves as a versatile chiral building block for the synthesis of bioactive molecules, enabling efficient introduction of a stereodefined iodoalkyl moiety. Its bench-stable tert-butyl carbamate protection facilitates straightforward handling and purification, while the iodomethyl group supports diverse transformations including Suzuki-Miyaura coupling, nucleophilic substitution, and transition-metal-catalyzed cross-couplings. This compound functions effectively in the construction of complex heterocyclic scaffolds and peptidomimetics under standard synthetic conditions.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: