3-Bromo-2,6-Difluoropyridine

≥98%

Reagent Code: #147203
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CAS Number 80392-79-6

science Other reagents with same CAS 80392-79-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.98 g/mol
Formula C₅H₂BrF₂N
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki and Negishi couplings to form carbon-carbon bonds in drug discovery. Also utilized in the preparation of kinase inhibitors and other biologically active compounds due to the electron-withdrawing nature of the halogens, which enhances reactivity and binding selectivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,740.00
5g
10-20 days ฿5,350.00
10g
10-20 days ฿9,470.00
25g
10-20 days ฿20,500.00
100g
10-20 days ฿76,440.00
3-Bromo-2,6-Difluoropyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki and Negishi couplings to form carbon-carbon bonds in drug discovery. Also utilized in the preparation of kinase inhibitors and other biologically active compounds due to the electron-wi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki and Negishi couplings to form carbon-carbon bonds in drug discovery. Also utilized in the preparation of kinase inhibitors and other biologically active compounds due to the electron-withdrawing nature of the halogens, which enhances reactivity and binding selectivity.

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