2-Bromo-4-fluoro-3-methoxypyridine

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Reagent Code: #129739
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CAS Number 1256819-71-2

science Other reagents with same CAS 1256819-71-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.01 g/mol
Formula C₆H₅BrFNO
badge Registry Numbers
MDL Number MFCD18257628
thermostat Physical Properties
Boiling Point 239.6±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.621±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 kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in drug discovery for introducing pyridine-based scaffolds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its halogenated aromatic core, which enhances binding affinity and metabolic stability.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,470.00
inventory 100mg
10-20 days ฿12,700.00

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2-Bromo-4-fluoro-3-methoxypyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in drug discovery for introducing pyridine-based scaffolds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its halogenated

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in drug discovery for introducing pyridine-based scaffolds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its halogenated aromatic core, which enhances binding affinity and metabolic stability.

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