Ethyl 3-(trifluoromethoxy)benzoate

98%

Reagent Code: #180643
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CAS Number 677713-01-8

science Other reagents with same CAS 677713-01-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.17 g/mol
Formula C₁₀H₉F₃O₃
badge Registry Numbers
MDL Number MFCD06204384
thermostat Physical Properties
Boiling Point 224.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require fluorinated aromatic structures. Its ester and trifluoromethoxy groups make it valuable in medicinal chemistry for enhancing metabolic stability and lipophilicity. Commonly employed in the preparation of analogs for structure-activity relationship (SAR) studies. Also utilized in the manufacture of certain herbicides and fungicides due to the electron-withdrawing nature of the trifluoromethoxy group, which can improve pesticidal activity. Suitable for use in cross-coupling reactions and other transformations in organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,390.00
inventory 250mg
10-20 days ฿27,290.00

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Ethyl 3-(trifluoromethoxy)benzoate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require fluorinated aromatic structures. Its ester and trifluoromethoxy groups make it valuable in medicinal chemistry for enhancing metabolic stability and lipophilicity. Commonly employed in the preparation of analogs for structure-activity relationship (SAR) studies. Also utilized in the manufacture of certain herbicides and fungicides due to the electron-withdrawi

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require fluorinated aromatic structures. Its ester and trifluoromethoxy groups make it valuable in medicinal chemistry for enhancing metabolic stability and lipophilicity. Commonly employed in the preparation of analogs for structure-activity relationship (SAR) studies. Also utilized in the manufacture of certain herbicides and fungicides due to the electron-withdrawing nature of the trifluoromethoxy group, which can improve pesticidal activity. Suitable for use in cross-coupling reactions and other transformations in organic synthesis.

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