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Structure of 205524-47-6
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(R)-Di-tert-butyl 5-oxopyrrolidine-1,2-dicarboxylate is a sterically hindered chiral synthon featuring a protected pyrrolidine core with a ketone at the C5 position. This configuration enables selective functionalization in asymmetric synthesis, particularly in the construction of nitrogen-containing heterocycles and peptidomimetics. The tert-butyl groups confer enhanced stability and solubility under standard bench conditions.
(R)-Di-tert-butyl 5-oxopyrrolidine-1,2-dicarboxylate serves as a versatile chiral synthon for the construction of pyrrolidine-based scaffolds in medicinal chemistry. Its sterically protected diester functionality enables selective transformations, including reduction to the corresponding amine derivative and subsequent coupling reactions. The molecule exhibits excellent bench stability and facilitates efficient purification, making it well-suited for multi-step synthesis and scale-up applications.
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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: