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Structure of 1638743-95-9
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This pyrrolidine derivative features a chiral scaffold with defined stereochemistry at the 2R,4S positions, enabling precise control in asymmetric synthesis. The tert-butyl and methyl ester groups enhance solubility and stability, while the hydroxymethyl side chain provides a handle for downstream functionalization. Ideal for constructing complex heterocyclic frameworks in medicinal chemistry and natural product synthesis.
1-tert-Butyl 2-methyl (2R,4S)-4-(hydroxymethyl)pyrrolidine-1,2-dicarboxylate serves as a stereochemically defined pyrrolidine building block for medicinal chemistry and natural product synthesis. The (2R,4S) configuration provides predictable reactivity in asymmetric synthesis, while the protected amine and ester functionalities enable orthogonal transformations. The hydroxymethyl group facilitates further functionalization via oxidation or coupling reactions. Bench-stable and readily purified by chromatography, it functions effectively in standard peptide and heterocyclic scaffold elaboration 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: