6-Chloro-4-iodopyridin-2-amine
95%
- Product Code: 120539
CAS:
1062608-73-4
| Molecular Weight: | 254.46 g./mol | Molecular Formula: | C₅H₄ClIN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28103329 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, sealed, dry, protected from light |
Product Description:
6-Chloro-4-iodopyridin-2-amine is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical compounds. Its structure, featuring both chloro and iodo substituents, makes it a valuable building block in the preparation of pharmaceuticals, particularly in the synthesis of heterocyclic compounds that exhibit biological activity.
In medicinal chemistry, it is often employed in the creation of potential drug candidates, especially those targeting neurological disorders or infectious diseases. The presence of halogen atoms allows for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the introduction of diverse molecular fragments.
Additionally, this compound is used in agrochemical research for the development of novel pesticides or herbicides, where its pyridine core can be modified to enhance efficacy and selectivity. Its role in material science is also notable, contributing to the synthesis of organic electronic materials or ligands for catalytic systems. Overall, its applications span across multiple fields, highlighting its importance in advanced chemical research and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,329.00 |
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| 0.250 | 10-20 days | ฿7,362.00 |
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| 1.000 | 10-20 days | ฿19,863.00 |
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6-Chloro-4-iodopyridin-2-amine
6-Chloro-4-iodopyridin-2-amine is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex chemical compounds. Its structure, featuring both chloro and iodo substituents, makes it a valuable building block in the preparation of pharmaceuticals, particularly in the synthesis of heterocyclic compounds that exhibit biological activity.
In medicinal chemistry, it is often employed in the creation of potential drug candidates, especially those targeting neurological disorders or infectious diseases. The presence of halogen atoms allows for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the introduction of diverse molecular fragments.
Additionally, this compound is used in agrochemical research for the development of novel pesticides or herbicides, where its pyridine core can be modified to enhance efficacy and selectivity. Its role in material science is also notable, contributing to the synthesis of organic electronic materials or ligands for catalytic systems. Overall, its applications span across multiple fields, highlighting its importance in advanced chemical research and development.
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