Methyl 2-(2,6-difluoro-3-nitrophenyl)acetate

97%

Reagent Code: #214294
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CAS Number 361336-79-0

science Other reagents with same CAS 361336-79-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.15 g/mol
Formula C₉H₇F₂NO₄
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where fluorine substitution enhances metabolic stability and bioavailability. Its nitro and ester functionalities allow for further chemical transformations, such as reductions and nucleophilic substitutions, making it valuable in constructing complex drug molecules. Commonly employed in research and development for agrochemicals and medicinal chemistry due to the combined electron-withdrawing effects of fluorine and nitro groups, which influence reactivity and binding characteristics.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿12,390.00
250mg
10-20 days ฿20,600.00
1g
10-20 days ฿51,490.00
Methyl 2-(2,6-difluoro-3-nitrophenyl)acetate
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Used as an intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where fluorine substitution enhances metabolic stability and bioavailability. Its nitro and ester functionalities allow for further chemical transformations, such as reductions and nucleophilic substitutions, making it valuable in constructing complex drug molecules. Commonly employed in research and development for agrochemicals and medicinal chemi

Used as an intermediate in the synthesis of fluorinated pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where fluorine substitution enhances metabolic stability and bioavailability. Its nitro and ester functionalities allow for further chemical transformations, such as reductions and nucleophilic substitutions, making it valuable in constructing complex drug molecules. Commonly employed in research and development for agrochemicals and medicinal chemistry due to the combined electron-withdrawing effects of fluorine and nitro groups, which influence reactivity and binding characteristics.

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