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

blur_circular Chemical Specifications

scatter_plot Molecular Information
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.

Available Sizes & Pricing

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