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Structure of 121148-00-3
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Methyl (2S,4R)-1-(tert-butoxycarbonyl)-4-aminopyrrolidine-2-carboxylate is a chiral pyrrolidine derivative featuring a protected amine and ester functionality. This scaffold integrates a stereodefined amino group flanked by a tert-butoxycarbonyl (Boc) protection, enabling selective transformations in peptide synthesis and medicinal chemistry workflows. The methyl ester moiety offers enhanced solubility and stability under standard conditions, facilitating downstream derivatization.
Methyl (2S,4R)-1-(tert-butoxycarbonyl)-4-aminopyrrolidine-2-carboxylate serves as a key chiral building block for pyrrolidine-based scaffolds in medicinal chemistry. The Boc-protected amine and ester functionalities enable sequential transformations, including deprotection, coupling, and cyclization reactions. Its stereochemical integrity supports reproducible synthesis of complex heterocycles, while the tert-butyl carbamate group offers stability and ease of purification under standard bench conditions.
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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: