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Structure of 125347-83-3
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1-(tert-Butyl) 2-ethyl pyrrolidine-1,2-dicarboxylate features a sterically hindered tert-butyl group paired with an ethyl substituent on the pyrrolidine ring, delivering enhanced stability and solubility in organic media. This configuration enables efficient incorporation into asymmetric synthesis workflows, where the dicarboxylate moiety serves as a robust chiral auxiliary for stereoselective transformations.
1-(tert-Butyl) 2-ethyl pyrrolidine-1,2-dicarboxylate serves as a versatile chiral building block in synthetic organic chemistry, enabling efficient access to substituted pyrrolidines via selective deprotection and functionalization. The tert-butyl ester group offers excellent bench stability and ease of removal under mild acidic conditions, while the ethyl ester supports orthogonal reactivity. This scaffold facilitates the construction of biologically relevant heterocycles and is well-suited for iterative synthesis strategies in medicinal chemistry and process development.
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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: