6-Bromo-4-fluoro-3-iodo-1H-indazole
98%
- Product Code: 79614
CAS:
887568-00-5
| Molecular Weight: | 340.92 g./mol | Molecular Formula: | C₇H₃BrFIN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07781844 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research as a versatile building block for the synthesis of more complex molecules. Its structure, featuring multiple halogen substituents, makes it a valuable intermediate in the development of potential drug candidates, particularly those targeting various diseases such as cancer, inflammation, and infectious diseases. The presence of bromo, fluoro, and iodo groups allows for selective chemical modifications, enabling researchers to explore structure-activity relationships and optimize the biological activity of the final compounds. Additionally, it is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create diverse indazole derivatives with potential therapeutic applications. Its role in the development of kinase inhibitors and other enzyme-targeting agents is also noteworthy, as indazole scaffolds are commonly found in biologically active molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft207,218.42 |
+
-
|
6-Bromo-4-fluoro-3-iodo-1H-indazole
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research as a versatile building block for the synthesis of more complex molecules. Its structure, featuring multiple halogen substituents, makes it a valuable intermediate in the development of potential drug candidates, particularly those targeting various diseases such as cancer, inflammation, and infectious diseases. The presence of bromo, fluoro, and iodo groups allows for selective chemical modifications, enabling researchers to explore structure-activity relationships and optimize the biological activity of the final compounds. Additionally, it is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create diverse indazole derivatives with potential therapeutic applications. Its role in the development of kinase inhibitors and other enzyme-targeting agents is also noteworthy, as indazole scaffolds are commonly found in biologically active molecules.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
Ft0.00
Ft0.00
Total :