Ethyl 3-fluoro-4-nitrobenzoate

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Reagent Code: #182573
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CAS Number 914347-91-4

science Other reagents with same CAS 914347-91-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.16 g/mol
Formula C₉H₈FNO₄
badge Registry Numbers
MDL Number MFCD07782042
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated active pharmaceutical ingredients (APIs) where the fluorine atom enhances metabolic stability and bioavailability. Its nitro group allows for further functionalization, such as reduction to an amine, enabling coupling reactions to form amides or heterocycles. Commonly employed in medicinal chemistry for constructing benzene-ring-based scaffolds in drug candidates targeting CNS disorders, inflammation, and infectious diseases. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿2,520.00
inventory 25g
10-20 days ฿5,980.00
inventory 100g
10-20 days ฿19,850.00
inventory 5g
10-20 days ฿1,350.00
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Ethyl 3-fluoro-4-nitrobenzoate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated active pharmaceutical ingredients (APIs) where the fluorine atom enhances metabolic stability and bioavailability. Its nitro group allows for further functionalization, such as reduction to an amine, enabling coupling reactions to form amides or heterocycles. Commonly employed in medicinal chemistry for constructing benzene-ring-based scaffolds in drug candidates targeting CNS disorders, inflammati

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated active pharmaceutical ingredients (APIs) where the fluorine atom enhances metabolic stability and bioavailability. Its nitro group allows for further functionalization, such as reduction to an amine, enabling coupling reactions to form amides or heterocycles. Commonly employed in medicinal chemistry for constructing benzene-ring-based scaffolds in drug candidates targeting CNS disorders, inflammation, and infectious diseases. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles.

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