Ethyl 2-fluoro-6-methylbenzoate

95%

Reagent Code: #182633
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CAS Number 90259-30-6

science Other reagents with same CAS 90259-30-6

blur_circular Chemical Specifications

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Weight 182.19 g/mol
Formula C₁₀H₁₁FO₂
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its ester functionality and fluorine substitution make it valuable in medicinal chemistry for enhancing metabolic stability and membrane permeability. Commonly employed in Suzuki and other cross-coupling reactions to build complex aromatic systems. Also utilized in agrochemical research for designing herbicides and fungicides due to the electron-withdrawing effect of the fluorine atom improving compound reactivity and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,890.00
inventory 1g
10-20 days ฿4,550.00
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Ethyl 2-fluoro-6-methylbenzoate
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its ester functionality and fluorine substitution make it valuable in medicinal chemistry for enhancing metabolic stability and membrane permeability. Commonly employed in Suzuki and other cross-coupling reactions to build complex aromatic systems. Also utilized in agrochemical research for designing herbicides and fun

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its ester functionality and fluorine substitution make it valuable in medicinal chemistry for enhancing metabolic stability and membrane permeability. Commonly employed in Suzuki and other cross-coupling reactions to build complex aromatic systems. Also utilized in agrochemical research for designing herbicides and fungicides due to the electron-withdrawing effect of the fluorine atom improving compound reactivity and selectivity.

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