4-Bromo-2-fluoro-3-(trifluoromethyl)pyridine

95%

Reagent Code: #152295
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CAS Number 1227496-58-3

science Other reagents with same CAS 1227496-58-3

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Weight 243.98 g/mol
Formula C₆H₂BrF₄N
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MDL Number MFCD16609975
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its halogenated pyridine structure makes it valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig aminations, enabling the construction of complex organic compounds. Commonly employed in the creation of herbicides, fungicides, and kinase inhibitors due to the electron-withdrawing properties and stability imparted by the trifluoromethyl and halogen substituents. Also utilized in materials science for designing organic semiconductors and liquid crystals where fluorinated aromatic systems enhance performance.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,400.00
inventory 250mg
10-20 days ฿12,580.00
inventory 1g
10-20 days ฿36,780.00

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4-Bromo-2-fluoro-3-(trifluoromethyl)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its halogenated pyridine structure makes it valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig aminations, enabling the construction of complex organic compounds. Commonly employed in the creation of herbicides, fungicides, and kinase inhibitors due to the electron-withdrawing properties and stability imparted by the trifluoromethyl and halogen su

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its halogenated pyridine structure makes it valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig aminations, enabling the construction of complex organic compounds. Commonly employed in the creation of herbicides, fungicides, and kinase inhibitors due to the electron-withdrawing properties and stability imparted by the trifluoromethyl and halogen substituents. Also utilized in materials science for designing organic semiconductors and liquid crystals where fluorinated aromatic systems enhance performance.

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