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Structure of 441717-40-4
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(R)-1-Boc-pyrrolidine-1,3-dicarboxylate features a stereochemically defined pyrrolidine core with orthogonal Boc and dicarboxylate functionalities. This configuration enables selective derivatization in asymmetric synthesis, particularly in peptide mimetics and catalyst design. The protected amine and stable ester groups facilitate sequential functionalization under standard conditions.
(R)-1-Boc-pyrrolidine-1,3-dicarboxylate serves as a key chiral building block in asymmetric synthesis, enabling efficient access to pyrrolidine-containing scaffolds. The Boc group provides excellent stability and ease of removal under mild acidic conditions, while the 1,3-dicarboxylate functionality supports orthogonal derivatization. This compound facilitates diverse transformations including reductive amination, cross-coupling, and heterocycle formation, making it highly valuable for medicinal chemistry and process development workflows.
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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: