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Structure of 895243-98-8
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This chiral pyrrolidine derivative features a 3-ethyl-4-amino substitution pattern on a bench-stable, tert-butyl-protected scaffold. The (3R,4S) stereochemistry enables precise control in asymmetric synthesis, particularly for peptide mimetics and bioactive heterocycles. Designed for efficient incorporation into complex molecular architectures under standard conditions.
(3R,4S)-1-tert-butyl 3-ethyl 4-aminopyrrolidine-1,3-dicarboxylate serves as a stereochemically defined pyrrolidine building block for medicinal chemistry and peptide mimicry. The protected amine and orthogonal ester functionalities enable sequential functionalization in multistep syntheses. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient access to complex heterocyclic scaffolds and bioactive intermediates.
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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: