6-Bromo-2-chloro-3-fluoropyridine

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Reagent Code: #151890
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CAS Number 1211591-93-3

science Other reagents with same CAS 1211591-93-3

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scatter_plot Molecular Information
Weight 210.43 g/mol
Formula C₅H₂BrClFN
badge Registry Numbers
MDL Number MFCD18257569
inventory_2 Storage & Handling
Storage 2-8°C

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 halogen substituents allow for selective cross-coupling reactions, making it valuable in building complex molecules through palladium-catalyzed reactions like Suzuki or Buchwald-Hartwig aminations. Commonly employed in the creation of herbicides, insecticides, and kinase inhibitors due to its ability to enhance metabolic stability and binding affinity in target compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,250.00
inventory 1g
10-20 days ฿3,080.00
inventory 5g
10-20 days ฿15,120.00
inventory 10g
10-20 days ฿29,650.00

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6-Bromo-2-chloro-3-fluoropyridine
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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 halogen substituents allow for selective cross-coupling reactions, making it valuable in building complex molecules through palladium-catalyzed reactions like Suzuki or Buchwald-Hartwig aminations. Commonly employed in the creation of herbicides, insecticides, and kinase inhibitors due to its ability to enhance metabolic stability and binding a

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its halogen substituents allow for selective cross-coupling reactions, making it valuable in building complex molecules through palladium-catalyzed reactions like Suzuki or Buchwald-Hartwig aminations. Commonly employed in the creation of herbicides, insecticides, and kinase inhibitors due to its ability to enhance metabolic stability and binding affinity in target compounds.

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