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Structure of 220652-51-7
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This chiral pyrrolidine derivative features a tert-butyl group and a methyl substituent at the 2-position, conferring enhanced steric bulk and stability. The (R)-configuration at the 2,5-dihydro-1H-pyrrole core enables stereoselective transformations in asymmetric synthesis. Its bench-stable nature and compatibility with standard reaction conditions make it a reliable building block for complex heterocyclic systems.
1-(tert-Butyl) 2-methyl (R)-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate serves as a stable, bench-ready chiral building block for the synthesis of pyrrolidine-based scaffolds. Its tert-butyl ester and methyl substituent provide excellent functional group tolerance and ease of purification, enabling efficient transformations in asymmetric synthesis. The (R)-configured dihydropyrrole core facilitates stereoselective coupling reactions and is well-suited for constructing medicinally relevant heterocyclic frameworks.
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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: