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*For research and further manufacturing use only, not for direct human use.
Structure of 121148-01-4
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This chiral pyrrolidine derivative features a tert-butyl-protected amine and methyl-substituted backbone, enabling direct incorporation into peptide-like scaffolds. The (2S,4S) stereochemistry ensures high diastereoselectivity in cycloadditions and coupling reactions, while the bench-stable, moisture-tolerant nature simplifies handling under standard conditions.
(2S,4S)-1-tert-butyl 2-methyl 4-aminopyrrolidine-1,2-dicarboxylate serves as a stereochemically defined pyrrolidine building block for medicinal chemistry and peptide-like scaffold synthesis. The protected amine and dicarboxylate groups enable sequential functionalization, while the tert-butyl and methyl substituents provide steric control and bench stability. It facilitates efficient access to chiral heterocycles via standard coupling, reduction, and cyclization protocols in multi-step syntheses.
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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: