(3R,4S)-4-(4-(Benzyloxy)phenyl)-1-(4-fluorophenyl)-3-(3-(4-fluorophenyl)-3-oxopropyl)azetidin-2-one

98%

Reagent Code: #230130
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CAS Number 190595-65-4

science Other reagents with same CAS 190595-65-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 497.53 g/mol
Formula C₃₁H₂₅F₂NO₃
thermostat Physical Properties
Boiling Point 706.8°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors. Its structural features enable selective binding in biological systems, making it valuable in research for antiviral agents, especially hepatitis C virus (HCV) treatments. The compound's stereochemistry and functional groups support high potency and specificity in target enzyme inhibition, facilitating advancement in drug candidates during preclinical stages.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿159.50
inventory 1g
10-20 days ฿258.50
inventory 5g
10-20 days ฿1,910.00
inventory 25g
10-20 days ฿7,010.00

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(3R,4S)-4-(4-(Benzyloxy)phenyl)-1-(4-fluorophenyl)-3-(3-(4-fluorophenyl)-3-oxopropyl)azetidin-2-one
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors. Its structural features enable selective binding in biological systems, making it valuable in research for antiviral agents, especially hepatitis C virus (HCV) treatments. The compound's stereochemistry and functional groups support high potency and specificity in target enzyme inhibition, facilitating advancement in drug candidates during preclinical stages.

Used in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors. Its structural features enable selective binding in biological systems, making it valuable in research for antiviral agents, especially hepatitis C virus (HCV) treatments. The compound's stereochemistry and functional groups support high potency and specificity in target enzyme inhibition, facilitating advancement in drug candidates during preclinical stages.

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