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Structure of 64700-65-8
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Methyl (R)-5-oxopyrrolidine-2-carboxylate is a chiral pyrrolidine derivative featuring a ketone at the C5 position and a methyl ester at C2. This configuration imparts high stereoselectivity in asymmetric synthesis, enabling efficient access to complex nitrogen-containing scaffolds. The compound exhibits excellent stability under standard bench conditions and integrates readily into diverse reaction sequences.
Methyl (R)-5-oxopyrrolidine-2-carboxylate serves as a versatile chiral building block in synthetic organic chemistry, enabling efficient access to pyrrolidine-based scaffolds. Its enantioselective synthesis and stable α-aminoketone functionality facilitate diverse transformations, including reductive amination, nucleophilic addition, and heterocycle construction. The ester group supports straightforward derivatization and purification, while the inherent stereochemistry simplifies downstream asymmetric synthesis. This compound functions as a key intermediate in the development of bioactive molecules and pharmaceutical candidates requiring defined stereochemistry.
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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: