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Structure of 83623-93-2
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This chiral pyrrolidine derivative features a tert-butoxycarbonyl-protected amine and a methoxy-substituted ring, offering a stable, bench-ready scaffold for peptide bond mimicry. The (2S,4S) stereochemistry ensures precise spatial orientation in synthetic sequences, enabling efficient incorporation into bioactive peptides and constrained molecular frameworks under standard conditions.
(2S,4S)-1-(tert-Butoxycarbonyl)-4-methoxypyrrolidine-2-carboxylic acid serves as a stereochemically defined building block for the synthesis of pyrrolidine-based peptidomimetics and bioactive heterocycles. The Boc group provides robust protection of the amine, enabling orthogonal manipulation with the pendant methoxy functionality. Its stability under standard coupling conditions and compatibility with diverse functional groups facilitate efficient access to complex scaffolds in 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: