3,5-Dibromo-2,6-difluoropyridine

97%

Reagent Code: #131786
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CAS Number 685517-84-4

science Other reagents with same CAS 685517-84-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.87 g/mol
Formula C₅HBr₂F₂N
badge Registry Numbers
MDL Number MFCD12756681
thermostat Physical Properties
Boiling Point 217.7±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.210±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

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 halogenated structure allows 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 and fungicides due to its ability to enhance bioavailability and stability in final products. Also utilized in research settings for designing novel compounds with targeted biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,550.00
inventory 1g
10-20 days ฿33,830.00

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3,5-Dibromo-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 halogenated structure allows 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 and fungicides due to its ability to enhance bioavailability and stability in final products. Also

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its halogenated structure allows 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 and fungicides due to its ability to enhance bioavailability and stability in final products. Also utilized in research settings for designing novel compounds with targeted biological activity.

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