tert-Butyl 3-iodo-2-methyl-6,7-dihydropyrazolo[1,5-a]pyrazine-5(4H)-carboxylate
95%
- Product Code: 83696
CAS:
2138122-16-2
| Molecular Weight: | 363.1935 g./mol | Molecular Formula: | C₁₂H₁₈IN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Widely utilized in pharmaceutical research, this compound serves as a key intermediate in the synthesis of biologically active molecules. Its structure is particularly valuable in the development of novel drug candidates, especially those targeting central nervous system disorders. The presence of the iodomethyl group allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for screening purposes. Additionally, the tert-butyl ester moiety provides protection for the carboxyl group during multi-step synthetic processes, ensuring selective reactivity at other sites. This compound's versatility makes it an essential building block in medicinal chemistry, particularly in the design of heterocyclic compounds with potential therapeutic applications. Its stability and reactivity profile also make it suitable for use in automated synthesis platforms, facilitating high-throughput drug discovery efforts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿7,200.00 |
+
-
|
| 0.100 | 10-20 days | ฿21,600.00 |
+
-
|
tert-Butyl 3-iodo-2-methyl-6,7-dihydropyrazolo[1,5-a]pyrazine-5(4H)-carboxylate
Widely utilized in pharmaceutical research, this compound serves as a key intermediate in the synthesis of biologically active molecules. Its structure is particularly valuable in the development of novel drug candidates, especially those targeting central nervous system disorders. The presence of the iodomethyl group allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for screening purposes. Additionally, the tert-butyl ester moiety provides protection for the carboxyl group during multi-step synthetic processes, ensuring selective reactivity at other sites. This compound's versatility makes it an essential building block in medicinal chemistry, particularly in the design of heterocyclic compounds with potential therapeutic applications. Its stability and reactivity profile also make it suitable for use in automated synthesis platforms, facilitating high-throughput drug discovery efforts.
| 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 :