2-Bromo-3-fluoro-4-methoxypyridine

98%

Reagent Code: #129327
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CAS Number 109613-98-1

science Other reagents with same CAS 109613-98-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.01 g/mol
Formula C₆H₅BrFNO
badge Registry Numbers
MDL Number MFCD18257613
thermostat Physical Properties
Boiling Point 223.2±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 an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-inflammatory agents. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in agrochemical research for creating novel pesticides and herbicides due to its electron-withdrawing properties and stability. Commonly utilized in Suzuki and Buchwald-Hartwig reactions to form carbon-carbon and carbon-nitrogen bonds in advanced organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,510.00
inventory 250mg
10-20 days ฿9,270.00
inventory 1g
10-20 days ฿18,820.00

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2-Bromo-3-fluoro-4-methoxypyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-inflammatory agents. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in agrochemical research for creating novel pesticides and herbicides due to its electron-withdrawing properties and stability. C

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-inflammatory agents. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Also employed in agrochemical research for creating novel pesticides and herbicides due to its electron-withdrawing properties and stability. Commonly utilized in Suzuki and Buchwald-Hartwig reactions to form carbon-carbon and carbon-nitrogen bonds in advanced organic synthesis.

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