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Structure of 113400-36-5
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This chiral pyrrolidine derivative features a tert-butyl group at the nitrogen and a benzyl ester at C2, delivering enhanced stability and solubility. The (S)-configuration enables stereocontrolled synthesis in complex molecule assembly. Its bench-stable nature simplifies handling during multistep transformations.
2-Benzyl 1-(tert-butyl) (S)-5-oxopyrrolidine-1,2-dicarboxylate serves as a versatile chiral building block in asymmetric synthesis, enabling efficient access to pyrrolidine-based scaffolds. Its tert-butyl and benzyl groups provide orthogonal protection for nitrogen and carboxyl functionalities, facilitating selective deprotection and functionalization. The molecule exhibits excellent bench stability and simplifies purification, making it well-suited for multi-step synthetic sequences in medicinal chemistry and process development.
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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: