5-Bromo-3-fluoro-2-iodopyridine

97%

Reagent Code: #152028
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CAS Number 1260665-95-9

science Other reagents with same CAS 1260665-95-9

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scatter_plot Molecular Information
Weight 301.88 g/mol
Formula C₅H₂BrFIN
badge Registry Numbers
MDL Number MFCD18250716
inventory_2 Storage & Handling
Storage 2-8°C, dry, light-proof

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 halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Buchwald-Hartwig aminations, enabling the construction of complex molecules in drug discovery. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance metabolic stability and binding affinity in target molecules. The compound’s versatility in forming carbon-heteroatom and carbon-carbon bonds makes it valuable in medicinal chemistry and process development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,200.00
inventory 250mg
10-20 days ฿8,860.00
inventory 1g
10-20 days ฿20,360.00

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5-Bromo-3-fluoro-2-iodopyridine
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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 halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Buchwald-Hartwig aminations, enabling the construction of complex molecules in drug discovery. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance metabolic stability and binding affinity in target m

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Buchwald-Hartwig aminations, enabling the construction of complex molecules in drug discovery. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance metabolic stability and binding affinity in target molecules. The compound’s versatility in forming carbon-heteroatom and carbon-carbon bonds makes it valuable in medicinal chemistry and process development.

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