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Structure of 35309-35-4
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Methyl 5-oxopyrrolidine-3-carboxylate is a versatile heterocyclic building block featuring a cyclic amide with a ketone at the C5 position and an ester at C3. This configuration enables direct functionalization at multiple sites, supporting efficient synthesis of pyrrolidine derivatives. The molecule exhibits enhanced stability under standard bench conditions and integrates readily into diverse reaction sequences.
Methyl 5-oxopyrrolidine-3-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to pyrrolidine-based scaffolds through reductive amination and subsequent functionalization. The molecule's α,β-unsaturated lactam moiety facilitates conjugate additions and cycloaddition reactions, while the methyl ester group offers orthogonal handle for selective transformations. Bench-stable and readily purified by flash chromatography, it functions effectively in medicinal chemistry campaigns targeting bioactive heterocycles and peptide mimetics.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: