3-bromo-6-fluoropyridine-2-carbonitrile

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Reagent Code: #141738
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CAS Number 1565634-54-9

science Other reagents with same CAS 1565634-54-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.9959 g/mol
Formula C₆H₂BrFN₂
badge Registry Numbers
MDL Number MFCD26904956
thermostat Physical Properties
Boiling Point 291.7±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.81±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce the pyridine core into target molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-withdrawing nitrile and halogen groups that enhance binding affinity and metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,000.00
inventory 250mg
10-20 days ฿32,000.00
inventory 1g
10-20 days ฿80,000.00

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3-bromo-6-fluoropyridine-2-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce the pyridine core into target molecules. Also utilized in agrochemical research for designing novel pes

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce the pyridine core into target molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-withdrawing nitrile and halogen groups that enhance binding affinity and metabolic stability.

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