2-Chloro-5-fluoropyrimidine

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Reagent Code: #158402
label
Alias 2-Chloro-5-Fluoropyrimidine
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CAS Number 62802-42-0

science Other reagents with same CAS 62802-42-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 132.52 g/mol
Formula C₄H₂ClFN₂
badge Registry Numbers
MDL Number MFCD03788197
thermostat Physical Properties
Boiling Point 149.0-162.0°C
inventory_2 Storage & Handling
Density 1.073 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for selective functionalization, making it valuable in constructing pyrimidine-based drug candidates. Commonly employed in cross-coupling reactions to introduce the pyrimidine core into larger bioactive molecules. Also utilized in agrochemical research for the design of novel pesticides and herbicides due to its electron-deficient ring system that enhances binding to biological targets.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿137.50
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿620.00
inventory 25g
10-20 days ฿2,700.00

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2-Chloro-5-fluoropyrimidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for selective functionalization, making it valuable in constructing pyrimidine-based drug candidates. Commonly employed in cross-coupling reactions to introduce the pyrimidine core into larger bioactive molecules. Also utilized in agrochemical research for the design of novel pesticides and herbicides due to its electron-deficient ring system that enhanc

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for selective functionalization, making it valuable in constructing pyrimidine-based drug candidates. Commonly employed in cross-coupling reactions to introduce the pyrimidine core into larger bioactive molecules. Also utilized in agrochemical research for the design of novel pesticides and herbicides due to its electron-deficient ring system that enhances binding to biological targets.

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