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Structure of 145681-01-2
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1-Tert-Butyl 2-methyl pyrrolidine-1,2-dicarboxylate features a sterically hindered pyrrolidine core with orthogonal ester handles, enabling selective deprotection and functionalization. The tert-butyl group provides exceptional stability under basic conditions, while the methyl substituent enhances regioselectivity in asymmetric synthesis. This robust scaffold facilitates efficient access to chiral intermediates for medicinal chemistry applications.
1-Tert-Butyl 2-methyl 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 facilitates straightforward purification, while the methyl substituent provides defined stereochemical control. It functions effectively in standard coupling reactions, cycloadditions, and transition-metal-catalyzed transformations, making it well-suited for medicinal chemistry and process development workflows.
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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: