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Structure of 335280-19-8
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This chiral pyrrolidine derivative features a tert-butyl ester-protected carboxylic acid and a hydroxyl group in the (2R,3R) stereoconfiguration. It serves as a key building block for synthesizing bioactive molecules, particularly in peptidomimetic and natural product frameworks. The molecule exhibits enhanced stability and solubility under standard bench conditions, enabling straightforward handling in synthetic workflows.
(2R,3R)-1-(tert-Butoxycarbonyl)-3-hydroxypyrrolidine-2-carboxylic acid serves as a stereochemically defined building block for the synthesis of pyrrolidine-based peptidomimetics and bioactive heterocycles. The protected amine and hydroxyl groups enable orthogonal functionalization, while the tert-butyl carbamate offers bench stability and ease of purification. This scaffold facilitates efficient coupling reactions and is compatible with standard peptide synthesis 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: