4-Iodo-1-methyl-1H-imidazole-5-carbaldehyde
95%
- Product Code: 47772
CAS:
189014-13-9
| Molecular Weight: | 236.0105 g./mol | Molecular Formula: | C₅H₅IN₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01632219 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. It is particularly valuable in the development of pharmaceuticals and bioactive compounds, where its structure allows for further functionalization. The iodine atom in the molecule serves as a reactive site for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. Additionally, the aldehyde group can undergo various transformations, including reductions, oxidations, or condensations, making it a key building block in medicinal chemistry. Its applications extend to the synthesis of imidazole-based drugs, which are often used in antifungal, antibacterial, and anticancer therapies. Researchers also explore its use in materials science for designing functional polymers or ligands in coordination chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €119.43 |
+
-
|
4-Iodo-1-methyl-1H-imidazole-5-carbaldehyde
This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex molecules. It is particularly valuable in the development of pharmaceuticals and bioactive compounds, where its structure allows for further functionalization. The iodine atom in the molecule serves as a reactive site for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds. Additionally, the aldehyde group can undergo various transformations, including reductions, oxidations, or condensations, making it a key building block in medicinal chemistry. Its applications extend to the synthesis of imidazole-based drugs, which are often used in antifungal, antibacterial, and anticancer therapies. Researchers also explore its use in materials science for designing functional polymers or ligands in coordination chemistry.
| 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:
€0.00
€0.00
Total :