6-Bromo-3-iodopyridin-2-amine

95%

Reagent Code: #149759
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CAS Number 1245643-34-8

science Other reagents with same CAS 1245643-34-8

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scatter_plot Molecular Information
Weight 298.91 g/mol
Formula C₅H₄BrIN₂
badge Registry Numbers
MDL Number MFCD18072576
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

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, enabling the construction of complex molecules in drug discovery. Commonly employed in palladium-catalyzed reactions such as Suzuki or Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for designing novel active ingredients. Its amine and halogen functional groups provide versatility in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,600.00
inventory 250mg
10-20 days ฿21,600.00
inventory 1g
10-20 days ฿44,760.00

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6-Bromo-3-iodopyridin-2-amine
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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, enabling the construction of complex molecules in drug discovery. Commonly employed in palladium-catalyzed reactions such as Suzuki or Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for designing novel active in

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, enabling the construction of complex molecules in drug discovery. Commonly employed in palladium-catalyzed reactions such as Suzuki or Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for designing novel active ingredients. Its amine and halogen functional groups provide versatility in multi-step synthetic routes.

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