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Structure of 92235-34-2
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tert-Butyl (S)-(2-oxopyrrolidin-3-yl)carbamate serves as a chiral building block for synthesizing pyrrolidine-based pharmaceuticals. This bench-stable, moisture-tolerant reagent features a protected (S)-configured pyrrolidin-3-one moiety, enabling direct incorporation into complex heterocycles via standard coupling protocols without racemization.
tert-Butyl (S)-(2-oxopyrrolidin-3-yl)carbamate serves as a chiral building block for the synthesis of pyrrolidine-based scaffolds, enabling efficient access to bioactive heterocycles. Its stable tert-butyl carbamate group facilitates straightforward protection and deprotection under mild acidic conditions, while the (S)-configured oxopyrrolidinyl moiety supports stereoselective transformations. The compound exhibits excellent functional group tolerance and is well-suited for iterative synthesis in medicinal chemistry workflows.
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Lot numbers can be found on the outside label of a product: