(4S)-3-[(5S)-5-(4-Fluorophenyl)-5-hydroxypentanoyl]-4-phenyl-1,3-oxazolidin-2-one

95%

Reagent Code: #234631
label
Alias (4S)-3-[(5S)-5-(4-fluorophenyl)-5-hydroxy-1-oxopentyl]-4-phenyl-2-ahzolidinone
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CAS Number 189028-95-3

science Other reagents with same CAS 189028-95-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 357.38 g/mol
Formula C₂₀H₂₀FNO₄
thermostat Physical Properties
Boiling Point 572.727ºC at 760 mmHg
inventory_2 Storage & Handling
Density 1.297
Storage Room temperature

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors. Its chiral structure makes it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in research settings for designing novel therapeutic agents, especially in antiviral and anticancer drug discovery. The compound's functional groups allow for selective modifications, enabling fine-tuning of biological activity in target molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿280.00
inventory 5g
10-20 days ฿400.00
inventory 25g
10-20 days ฿1,940.00
inventory 100g
10-20 days ฿5,880.00
(4S)-3-[(5S)-5-(4-Fluorophenyl)-5-hydroxypentanoyl]-4-phenyl-1,3-oxazolidin-2-one
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors. Its chiral structure makes it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in research settings for designing novel therapeutic agents, especially in antiviral and anticancer drug discovery. The compound's functional groups allow for selective modifications, enabling fine-tuning of biological activity in target molecules.

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors. Its chiral structure makes it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in research settings for designing novel therapeutic agents, especially in antiviral and anticancer drug discovery. The compound's functional groups allow for selective modifications, enabling fine-tuning of biological activity in target molecules.

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