6-Bromo-5-iodopyridin-2-amine

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Reagent Code: #87663
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CAS Number 1806995-70-9

science Other reagents with same CAS 1806995-70-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.91 g/mol
Formula C₅H₄BrIN₂
badge Registry Numbers
MDL Number MFCD22570450
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex chemical structures. Its unique halogenated pyridine structure makes it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other biologically active compounds. Researchers often employ it in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create diverse heterocyclic frameworks. Additionally, its amine group allows for further functionalization, enabling the creation of targeted molecules for drug discovery and material science applications. Its role in medicinal chemistry is notable, as it contributes to the development of potential therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿693.00
inventory 250mg
10-20 days ฿846.00
inventory 1g
10-20 days ฿2,367.00
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6-Bromo-5-iodopyridin-2-amine
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This compound is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex chemical structures. Its unique halogenated pyridine structure makes it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other biologically active compounds. Researchers often employ it in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create diverse heterocyclic frameworks. Additionally, its amine group allo

This compound is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex chemical structures. Its unique halogenated pyridine structure makes it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other biologically active compounds. Researchers often employ it in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create diverse heterocyclic frameworks. Additionally, its amine group allows for further functionalization, enabling the creation of targeted molecules for drug discovery and material science applications. Its role in medicinal chemistry is notable, as it contributes to the development of potential therapeutic agents.

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