3-Fluoro-4-iodopicolinonitrile

≥95%

Reagent Code: #117694
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CAS Number 669066-35-7

science Other reagents with same CAS 669066-35-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.00 g/mol
Formula C₆H₂FIN₂
badge Registry Numbers
MDL Number MFCD18633096
thermostat Physical Properties
Boiling Point 281.8±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds. Its structure allows for further functionalization, making it valuable in developing potential drug candidates, particularly for targeting neurological disorders and cancer. Also employed in agrochemical research to create novel pesticides and herbicides. Its unique fluorine and iodine substitutions enhance its reactivity, enabling the design of compounds with improved efficacy and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,504.00
inventory 1g
10-20 days ฿23,742.00
inventory 5g
10-20 days ฿82,251.00

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3-Fluoro-4-iodopicolinonitrile
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds. Its structure allows for further functionalization, making it valuable in developing potential drug candidates, particularly for targeting neurological disorders and cancer. Also employed in agrochemical research to create novel pesticides and herbicides. Its unique fluorine and iodine substitutions enhance its reactivity, enabling the design of compounds with improved efficacy and selectivity.
Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds. Its structure allows for further functionalization, making it valuable in developing potential drug candidates, particularly for targeting neurological disorders and cancer. Also employed in agrochemical research to create novel pesticides and herbicides. Its unique fluorine and iodine substitutions enhance its reactivity, enabling the design of compounds with improved efficacy and selectivity.
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