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Structure of 6404-31-5
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(R)-1-(benzyloxycarbonyl)pyrrolidine-2-carboxylic acid features a chiral pyrrolidine core with a benzylcarbamate protecting group, enabling selective incorporation into peptide sequences. This bench-stable derivative delivers precise stereochemical control in synthetic peptide workflows and supports efficient coupling under standard conditions.
(R)-1-(benzyloxycarbonyl)pyrrolidine-2-carboxylic acid serves as a stereochemically defined building block for the synthesis of peptidomimetics and bioactive heterocycles. Its benzyloxycarbonyl (Cbz) group provides orthogonal protection for the amine, enabling selective deprotection during peptide coupling sequences. The pyrrolidine-2-carboxylic acid scaffold exhibits excellent functional group tolerance and bench stability, facilitating efficient incorporation into complex molecular architectures via standard amide bond formation and catalytic transformations.
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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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: