6-Bromo-5-iodopyridin-2-amine
95%
- Product Code: 87663
CAS:
1806995-70-9
| Molecular Weight: | 298.91 g./mol | Molecular Formula: | C₅H₄BrIN₂ |
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| EC Number: | MDL Number: | MFCD22570450 | |
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| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $20.79 |
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| 0.250 | 10-20 days | $25.38 |
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| 1.000 | 10-20 days | $71.02 |
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6-Bromo-5-iodopyridin-2-amine
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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