3-Fluoro-4-nitrobenzonitrile

98%

Reagent Code: #81069
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CAS Number 218632-01-0

science Other reagents with same CAS 218632-01-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.11 g/mol
Formula C₇H₃FN₂O₂
thermostat Physical Properties
Melting Point 72-73°C
Boiling Point 316.4°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used primarily in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a key intermediate. Its structure allows for the introduction of fluorine and nitro groups into complex molecules, enhancing their biological activity. It is particularly valuable in the development of herbicides and fungicides, where the nitro group aids in binding to target enzymes. Additionally, it finds application in organic synthesis for creating heterocyclic compounds, which are crucial in drug discovery. Its reactivity makes it a versatile building block in medicinal chemistry for designing molecules with specific therapeutic properties.

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Test Parameter Specification
Appearance solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿620.00
inventory 5g
10-20 days ฿1,460.00
inventory 25g
10-20 days ฿6,640.00

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3-Fluoro-4-nitrobenzonitrile
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Used primarily in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a key intermediate. Its structure allows for the introduction of fluorine and nitro groups into complex molecules, enhancing their biological activity. It is particularly valuable in the development of herbicides and fungicides, where the nitro group aids in binding to target enzymes. Additionally, it finds application in organic synthesis for creating heterocyclic compounds, which are crucial in drug discovery.

Used primarily in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a key intermediate. Its structure allows for the introduction of fluorine and nitro groups into complex molecules, enhancing their biological activity. It is particularly valuable in the development of herbicides and fungicides, where the nitro group aids in binding to target enzymes. Additionally, it finds application in organic synthesis for creating heterocyclic compounds, which are crucial in drug discovery. Its reactivity makes it a versatile building block in medicinal chemistry for designing molecules with specific therapeutic properties.

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