(S)-tert-Butyl (2-oxopyrrolidin-3-yl)carbamate

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Reagent Code: #235076
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CAS Number 92235-34-2

science Other reagents with same CAS 92235-34-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.24 g/mol
Formula C₉H₁₆N₂O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of nootropic drugs like piracetam and related racetam family compounds. Its protected amine and ketone functional groups allow selective reactions in multi-step organic syntheses. Commonly employed in asymmetric synthesis due to the stereochemistry at the 3-position of the pyrrolidone ring, enabling the development of enantiomerically pure active pharmaceutical ingredients. Also utilized in the preparation of enzyme inhibitors and cognitive enhancers.

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Test Parameter Specification
Appearance white solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿710.00
inventory 100mg
10-20 days ฿1,350.00
inventory 250mg
10-20 days ฿2,260.00
inventory 1g
10-20 days ฿7,650.00
inventory 5g
10-20 days ฿38,250.00

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(S)-tert-Butyl (2-oxopyrrolidin-3-yl)carbamate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of nootropic drugs like piracetam and related racetam family compounds. Its protected amine and ketone functional groups allow selective reactions in multi-step organic syntheses. Commonly employed in asymmetric synthesis due to the stereochemistry at the 3-position of the pyrrolidone ring, enabling the development of enantiomerically pure active pharmaceutical ingredients. Also utilized in the preparation o

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of nootropic drugs like piracetam and related racetam family compounds. Its protected amine and ketone functional groups allow selective reactions in multi-step organic syntheses. Commonly employed in asymmetric synthesis due to the stereochemistry at the 3-position of the pyrrolidone ring, enabling the development of enantiomerically pure active pharmaceutical ingredients. Also utilized in the preparation of enzyme inhibitors and cognitive enhancers.

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