(S)-Benzyl 5-oxopyrrolidine-2-carboxylate

97%

Reagent Code: #237068
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CAS Number 94885-52-6

science Other reagents with same CAS 94885-52-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.24 g/mol
Formula C₁₂H₁₃NO₃
badge Registry Numbers
MDL Number MFCD14635629
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the production of antiviral and antidiabetic drugs. Its chiral structure makes it valuable for developing enantiomerically pure active pharmaceutical ingredients. Commonly employed in peptide-like backbone construction due to its pyrrolidine core and functionalized ester group, facilitating coupling reactions in multi-step organic syntheses. Also utilized in research settings for designing protease inhibitors and other biologically active molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,560.00
inventory 1g
10-20 days ฿4,200.00
inventory 5g
10-20 days ฿17,150.00
(S)-Benzyl 5-oxopyrrolidine-2-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the production of antiviral and antidiabetic drugs. Its chiral structure makes it valuable for developing enantiomerically pure active pharmaceutical ingredients. Commonly employed in peptide-like backbone construction due to its pyrrolidine core and functionalized ester group, facilitating coupling reactions in multi-step organic syntheses. Also utilized in research settings for designing protease inhibitors and other

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the production of antiviral and antidiabetic drugs. Its chiral structure makes it valuable for developing enantiomerically pure active pharmaceutical ingredients. Commonly employed in peptide-like backbone construction due to its pyrrolidine core and functionalized ester group, facilitating coupling reactions in multi-step organic syntheses. Also utilized in research settings for designing protease inhibitors and other biologically active molecules.

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