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

97%

Reagent Code: #113247
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CAS Number 163222-32-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 499.55 g/mol
Formula C₃₁H₂₇F₂NO₃
badge Registry Numbers
MDL Number MFCD00937870
thermostat Physical Properties
Boiling Point 706.462°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in pharmaceutical research, particularly in the development of enzyme inhibitors. It has shown potential in targeting specific enzymes involved in inflammatory and metabolic disorders. Its unique structure allows it to interact with enzyme active sites, making it a candidate for drug development in conditions like diabetes and autoimmune diseases. Additionally, its fluorophenyl and benzyloxy groups contribute to its stability and binding affinity, enhancing its efficacy in preclinical studies. Researchers are exploring its use in creating novel therapeutic agents with improved selectivity and reduced side effects.

format_list_bulleted Product Specification

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 1g
10-20 days ฿5,070.00
inventory 250mg
10-20 days ฿2,530.00
inventory 5g
10-20 days ฿13,700.00
(3R,4S)-4-(4-(Benzyloxy)phenyl)-1-(4-fluorophenyl)-3-((S)-3-(4-fluorophenyl)-3-hydroxypropyl)azetidin-2-one
This compound is primarily utilized in pharmaceutical research, particularly in the development of enzyme inhibitors. It has shown potential in targeting specific enzymes involved in inflammatory and metabolic disorders. Its unique structure allows it to interact with enzyme active sites, making it a candidate for drug development in conditions like diabetes and autoimmune diseases. Additionally, its fluorophenyl and benzyloxy groups contribute to its stability and binding affinity, enhancing its efficacy in preclinical studies. Researchers are exploring its use in creating novel therapeutic agents with improved selectivity and reduced side effects.
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