(S)-5-Oxo-1-((S)-1-phenylethyl)pyrrolidine-3-carboxylic acid

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Reagent Code: #235870
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CAS Number 173340-19-7

science Other reagents with same CAS 173340-19-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.2631 g/mol
Formula C₁₃H₁₅NO₃
badge Registry Numbers
MDL Number MFCD03427553
thermostat Physical Properties
Melting Point 204 - 211 ℃
Boiling Point 460.1 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.267±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable for asymmetric synthesis, where it helps control the formation of specific enantiomers in drug candidates. Commonly employed in medicinal chemistry for constructing complex cyclic frameworks found in neuroprotective agents and antiviral compounds. Also utilized in the preparation of enzyme inhibitors due to its structural similarity to proline derivatives, which are known to modulate enzymatic activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,500.00
inventory 1g
10-20 days ฿6,100.00
inventory 5g
10-20 days ฿24,820.00
(S)-5-Oxo-1-((S)-1-phenylethyl)pyrrolidine-3-carboxylic acid
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable for asymmetric synthesis, where it helps control the formation of specific enantiomers in drug candidates. Commonly employed in medicinal chemistry for constructing complex cyclic frameworks found in neuroprotective agents and antiviral compounds. Also utilized in the preparation of enzyme inhibitors due to its structur
Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable for asymmetric synthesis, where it helps control the formation of specific enantiomers in drug candidates. Commonly employed in medicinal chemistry for constructing complex cyclic frameworks found in neuroprotective agents and antiviral compounds. Also utilized in the preparation of enzyme inhibitors due to its structural similarity to proline derivatives, which are known to modulate enzymatic activity.
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