(R)-Benzyl (2,5-dioxopyrrolidin-3-yl)carbamate

97%

Reagent Code: #228755
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CAS Number 179747-84-3

science Other reagents with same CAS 179747-84-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.23 g/mol
Formula C₁₂H₁₂N₂O₄
badge Registry Numbers
MDL Number MFCD06796620
thermostat Physical Properties
Boiling Point 515.1±49.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.35±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports peptide-like frameworks, making it valuable in medicinal chemistry for creating enantiomerically pure compounds. Commonly employed in solid-phase synthesis and as an intermediate in the preparation of drug candidates targeting neurological disorders and viral infections. Also utilized in the design of enzyme inhibitors due to its ability to mimic transition states in peptide bond hydrolysis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,630.00
inventory 1g
10-20 days ฿20,600.00
inventory 5g
10-20 days ฿72,080.00
(R)-Benzyl (2,5-dioxopyrrolidin-3-yl)carbamate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports peptide-like frameworks, making it valuable in medicinal chemistry for creating enantiomerically pure compounds. Commonly employed in solid-phase synthesis and as an intermediate in the preparation of drug candidates targeting neurological disorders and viral infections. Also utilized in the design of enzyme inhibitors due to its

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports peptide-like frameworks, making it valuable in medicinal chemistry for creating enantiomerically pure compounds. Commonly employed in solid-phase synthesis and as an intermediate in the preparation of drug candidates targeting neurological disorders and viral infections. Also utilized in the design of enzyme inhibitors due to its ability to mimic transition states in peptide bond hydrolysis.

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