methyl 2-methyl-2-(3-(trifluoromethoxy)phenyl)propanoate

95%

Reagent Code: #209300

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 a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with central nervous system activity. Its structure supports the creation of chiral molecules, making it valuable in asymmetric synthesis for drugs targeting neurological disorders. Also employed in the preparation of agrochemicals due to the stability and reactivity imparted by the trifluoromethoxy group. The ester functionality allows for easy transformation into carboxylic acids, amides, or alcohols, enabling diverse derivatization in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿1,980.00
inventory 1g
10-20 days ฿6,480.00

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methyl 2-methyl-2-(3-(trifluoromethoxy)phenyl)propanoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with central nervous system activity. Its structure supports the creation of chiral molecules, making it valuable in asymmetric synthesis for drugs targeting neurological disorders. Also employed in the preparation of agrochemicals due to the stability and reactivity imparted by the trifluoromethoxy group. The ester functionality allows for easy transformation into c

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with central nervous system activity. Its structure supports the creation of chiral molecules, making it valuable in asymmetric synthesis for drugs targeting neurological disorders. Also employed in the preparation of agrochemicals due to the stability and reactivity imparted by the trifluoromethoxy group. The ester functionality allows for easy transformation into carboxylic acids, amides, or alcohols, enabling diverse derivatization in medicinal chemistry research.

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