ethyl trans-1-benzyl-4-(trifluoromethyl)pyrrolidine-3-carboxylate

98%

Reagent Code: #106588
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CAS Number 152188-51-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.3 g/mol
Formula C₁₅H₁₈F₃NO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a trifluoromethyl group and a benzyl moiety, makes it a valuable building block for developing potential drug candidates, particularly in the design of enzyme inhibitors or receptor modulators. The trifluoromethyl group enhances the compound's metabolic stability and binding affinity, which is crucial in drug discovery. Researchers often employ it in the creation of compounds targeting neurological disorders, inflammation, or infectious diseases due to its ability to interact with specific biological targets. Additionally, its pyrrolidine core is advantageous for constructing molecules with improved pharmacokinetic properties.

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Test Parameter Specification
Appearance Colorless Liquid
Purity (%) 97.5-100
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days £268.46
inventory bulk
10-20 days £0.00
inventory 1g
10-20 days £309.84
inventory 5g
10-20 days £919.40
ethyl trans-1-benzyl-4-(trifluoromethyl)pyrrolidine-3-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a trifluoromethyl group and a benzyl moiety, makes it a valuable building block for developing potential drug candidates, particularly in the design of enzyme inhibitors or receptor modulators. The trifluoromethyl group enhances the compound's metabolic stability and binding affinity, which is crucial in drug discovery. Researchers often employ it in the creation of compounds targeting neurological disorders, inflammation, or infectious diseases due to its ability to interact with specific biological targets. Additionally, its pyrrolidine core is advantageous for constructing molecules with improved pharmacokinetic properties.
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