Ethyl 4-iodo-1H-imidazole-2-carboxylate
95%
- Product Code: 47773
CAS:
1824103-80-1
| Molecular Weight: | 266.0365 g./mol | Molecular Formula: | C₆H₇IN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of imidazole-based compounds, which are known for their diverse biological activities. The iodine atom in the structure makes it a valuable candidate for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira reactions, enabling the creation of novel drug candidates. Additionally, its imidazole core is often exploited in the design of compounds targeting enzymes or receptors, making it relevant in the discovery of potential therapeutics for conditions like inflammation, infections, or cancer. Its ester group also allows for easy modification, facilitating the synthesis of derivatives with enhanced properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿5,346.00 |
+
-
|
Ethyl 4-iodo-1H-imidazole-2-carboxylate
This compound is primarily used in organic synthesis as a building block for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of imidazole-based compounds, which are known for their diverse biological activities. The iodine atom in the structure makes it a valuable candidate for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira reactions, enabling the creation of novel drug candidates. Additionally, its imidazole core is often exploited in the design of compounds targeting enzymes or receptors, making it relevant in the discovery of potential therapeutics for conditions like inflammation, infections, or cancer. Its ester group also allows for easy modification, facilitating the synthesis of derivatives with enhanced properties.
| 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 :