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Structure of 336818-78-1
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This chiral pyrrolidine derivative features a tert-butoxycarbonyl-protected amine and a phenyl-substituted C4 position, enabling direct incorporation into peptide synthesis. The stereochemistry at C2 and C4 ensures high diastereoselectivity in coupling reactions. Bench-stable and moisture-tolerant, it streamlines the assembly of complex peptidomimetics under standard conditions.
(2S,4R)-1-[(tert-Butoxy)carbonyl]-4-phenylpyrrolidine-2-carboxylic acid serves as a stereochemically defined pyrrolidine building block for medicinal chemistry applications. The Boc-protected amine and carboxylic acid functionalities enable sequential coupling reactions, while the phenyl-substituted pyrrolidine core provides structural rigidity and favorable physicochemical properties. Bench-stable and compatible with standard peptide synthesis protocols, it facilitates efficient access to complex heterocyclic scaffolds and bioactive molecules.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: