2-bromo-3-fluoropyridine-4-carbaldehyde

≥95%

Reagent Code: #144060
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CAS Number 1227572-94-2

science Other reagents with same CAS sdsdf1227572-94-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.00 g/mol
Formula C₆H₃BrFNO
badge Registry Numbers
MDL Number MFCD16606504
thermostat Physical Properties
Boiling Point 253.3±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.778±0.06 g/cm3(Predicted)
Storage -20°C, 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 creating compounds with high biological activity. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and stability. Its aldehyde group enables easy conversion into various derivatives like alcohols, acids, or imines, expanding its utility in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,160.00
inventory 5g
10-20 days ฿15,360.00
inventory 25g
10-20 days ฿48,000.00

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2-bromo-3-fluoropyridine-4-carbaldehyde
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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 creating compounds with high biological activity. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance mo

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 creating compounds with high biological activity. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and stability. Its aldehyde group enables easy conversion into various derivatives like alcohols, acids, or imines, expanding its utility in medicinal chemistry.

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