ethyl 2-(4-(trifluoromethoxy)phenyl)propanoate

90%

Reagent Code: #183935

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.08 g/mol
Formula C₁₂H₁₃F₃O₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory agents and central nervous system drugs such as antidepressants and analgesics. The trifluoromethoxy group enhances cell membrane permeability, metabolic stability, and biological target specificity, thereby improving efficacy and reducing side effects. Its chiral structure at the alpha position supports asymmetric synthesis, making it valuable in the production of enantiomerically pure drug molecules. Also employed in the preparation of agrochemicals and specialty materials due to the stability and reactivity imparted by the trifluoromethoxy group. Additionally utilized in organic chemistry research to develop new derivatives for pharmacological evaluation.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,290.00
inventory 1g
10-20 days ฿8,510.00
inventory 100mg
10-20 days ฿2,030.00

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ethyl 2-(4-(trifluoromethoxy)phenyl)propanoate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory agents and central nervous system drugs such as antidepressants and analgesics. The trifluoromethoxy group enhances cell membrane permeability, metabolic stability, and biological target specificity, thereby improving efficacy and reducing side effects. Its chiral structure at the alpha position supports asymmetric synthesis, making it valuable in the production of enantiomerically pure drug mol
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory agents and central nervous system drugs such as antidepressants and analgesics. The trifluoromethoxy group enhances cell membrane permeability, metabolic stability, and biological target specificity, thereby improving efficacy and reducing side effects. Its chiral structure at the alpha position supports asymmetric synthesis, making it valuable in the production of enantiomerically pure drug molecules. Also employed in the preparation of agrochemicals and specialty materials due to the stability and reactivity imparted by the trifluoromethoxy group. Additionally utilized in organic chemistry research to develop new derivatives for pharmacological evaluation.
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