(R)-Ethyl2,5-dioxo-3-(1H-pyrrol-1-yl)pyrrolidine-3-carboxylate

Reagent Code: #230775
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CAS Number 159213-19-1

science Other reagents with same CAS 159213-19-1

blur_circular Chemical Specifications

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Weight 236.22 g/mol
Formula C₁₁H₁₂N₂O₄
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used in pharmaceutical research as a chiral intermediate for synthesizing biologically active compounds, particularly in the development of protease inhibitors and other enzyme-targeted drugs. Its pyrrolidine-dione structure supports molecular diversity in medicinal chemistry, enabling the exploration of new drug candidates. Commonly employed in asymmetric synthesis due to its stereochemical purity, facilitating the production of enantiomerically enriched molecules. Also utilized in the preparation of peptide mimetics and heterocyclic scaffolds for drug discovery.

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inventory 100mg
10-20 days ฿11,780.00

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(R)-Ethyl2,5-dioxo-3-(1H-pyrrol-1-yl)pyrrolidine-3-carboxylate
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Used in pharmaceutical research as a chiral intermediate for synthesizing biologically active compounds, particularly in the development of protease inhibitors and other enzyme-targeted drugs. Its pyrrolidine-dione structure supports molecular diversity in medicinal chemistry, enabling the exploration of new drug candidates. Commonly employed in asymmetric synthesis due to its stereochemical purity, facilitating the production of enantiomerically enriched molecules. Also utilized in the preparation of pe

Used in pharmaceutical research as a chiral intermediate for synthesizing biologically active compounds, particularly in the development of protease inhibitors and other enzyme-targeted drugs. Its pyrrolidine-dione structure supports molecular diversity in medicinal chemistry, enabling the exploration of new drug candidates. Commonly employed in asymmetric synthesis due to its stereochemical purity, facilitating the production of enantiomerically enriched molecules. Also utilized in the preparation of peptide mimetics and heterocyclic scaffolds for drug discovery.

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