Ethyl 2-(4-(trifluoromethyl)pyridin-2-yl)acetate

≥95%

Reagent Code: #115711
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CAS Number 1189770-53-3

science Other reagents with same CAS 1189770-53-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.19 g/mol
Formula C₁₀H₁₀F₃NO₂
badge Registry Numbers
MDL Number MFCD26521232
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily used in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. In pharmaceuticals, it serves as a building block for the development of active pharmaceutical ingredients (APIs), particularly those targeting neurological and metabolic disorders. Its trifluoromethyl group enhances the biological activity and stability of the resulting compounds. In agrochemicals, it is utilized to create pesticides and herbicides, where the pyridine ring contributes to the effectiveness of these products in pest and weed control. Additionally, its ester functional group makes it a versatile reagent in organic synthesis, enabling further modifications to create diverse chemical structures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,662.00
inventory 100mg
10-20 days ฿2,331.00

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Ethyl 2-(4-(trifluoromethyl)pyridin-2-yl)acetate
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This chemical is primarily used in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. In pharmaceuticals, it serves as a building block for the development of active pharmaceutical ingredients (APIs), particularly those targeting neurological and metabolic disorders. Its trifluoromethyl group enhances the biological activity and stability of the resulting compounds. In agrochemicals, it is utilized to create pesticides and herbicides, where th

This chemical is primarily used in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. In pharmaceuticals, it serves as a building block for the development of active pharmaceutical ingredients (APIs), particularly those targeting neurological and metabolic disorders. Its trifluoromethyl group enhances the biological activity and stability of the resulting compounds. In agrochemicals, it is utilized to create pesticides and herbicides, where the pyridine ring contributes to the effectiveness of these products in pest and weed control. Additionally, its ester functional group makes it a versatile reagent in organic synthesis, enabling further modifications to create diverse chemical structures.

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