Methyl 4-fluoro-3-methylbenzoate

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Reagent Code: #205606
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CAS Number 180636-50-4

science Other reagents with same CAS 180636-50-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.16 g/mol
Formula C₉H₉FO₂
badge Registry Numbers
MDL Number MFCD06203783
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where fluorinated aromatic compounds enhance metabolic stability and bioavailability. It serves as a building block in the preparation of anti-inflammatory, analgesic, and central nervous system agents. Its ester functionality allows for further chemical modifications, enabling the formation of carboxylic acids, amides, or alcohols in multi-step organic syntheses. Also employed in agrochemical research for designing novel pesticides and herbicides due to the electron-withdrawing effect of the fluorine atom, which can improve compound efficacy and environmental stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10g
10-20 days ฿2,160.00
25g
10-20 days ฿4,710.00
100g
10-20 days ฿16,520.00
Methyl 4-fluoro-3-methylbenzoate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where fluorinated aromatic compounds enhance metabolic stability and bioavailability. It serves as a building block in the preparation of anti-inflammatory, analgesic, and central nervous system agents. Its ester functionality allows for further chemical modifications, enabling the formation of carboxylic acids, amides, or alcohols in multi-step organic syntheses. Also

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where fluorinated aromatic compounds enhance metabolic stability and bioavailability. It serves as a building block in the preparation of anti-inflammatory, analgesic, and central nervous system agents. Its ester functionality allows for further chemical modifications, enabling the formation of carboxylic acids, amides, or alcohols in multi-step organic syntheses. Also employed in agrochemical research for designing novel pesticides and herbicides due to the electron-withdrawing effect of the fluorine atom, which can improve compound efficacy and environmental stability.

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