3-Bromo-2-fluoro-6-methoxypyridine

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Reagent Code: #151348
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CAS Number 1227599-27-0

science Other reagents with same CAS 1227599-27-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.01 g/mol
Formula C₆H₅BrFNO
badge Registry Numbers
MDL Number MFCD16609956
thermostat Physical Properties
Boiling Point 192.2±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.621±0.06 g/cm3(Predicted)
Storage 2-8°C, 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) where halogenated pyridines enhance biological activity. Its structure allows for selective functionalization, making it valuable in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Commonly employed in the production of herbicides, fungicides, and kinase inhibitors due to the combined electronic effects of bromo, fluoro, and methoxy groups. Also utilized in research for building complex heterocyclic systems in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,130.00
inventory 5g
10-20 days ฿7,450.00
inventory 25g
10-20 days ฿26,070.00
inventory 100g
10-20 days ฿93,170.00

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3-Bromo-2-fluoro-6-methoxypyridine
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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) where halogenated pyridines enhance biological activity. Its structure allows for selective functionalization, making it valuable in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Commonly employed in the production of herbicides, fungicides, and kinase inhibitors due to the combined electronic effects of bromo, fluoro, and met
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs) where halogenated pyridines enhance biological activity. Its structure allows for selective functionalization, making it valuable in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Commonly employed in the production of herbicides, fungicides, and kinase inhibitors due to the combined electronic effects of bromo, fluoro, and methoxy groups. Also utilized in research for building complex heterocyclic systems in medicinal chemistry.
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