4-nitrobenzyl 2-(((tert-butyldimethylsilyl)oxy)methyl)-6,7-dihydropyrazolo[1,5-a]pyrazine-5(4H)-carboxylate
95%
- Product Code: 83843
CAS:
2460029-00-7
| Molecular Weight: | 446.571 g./mol | Molecular Formula: | C₂₁H₃₀N₄O₅Si |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry as a protected intermediate. It serves as a key building block in the development of more complex molecules, particularly in the synthesis of biologically active compounds. The tert-butyldimethylsilyl (TBDMS) group acts as a protective moiety for hydroxyl functionalities, ensuring selective reactivity during multi-step synthetic processes. Its nitrobenzyl component can be leveraged in photochemical applications, where it acts as a photolabile protecting group, allowing controlled release of active compounds under specific light conditions. This makes it valuable in the design of prodrugs or targeted drug delivery systems. Additionally, its pyrazolo[1,5-a]pyrazine core structure is of interest in the development of pharmaceuticals, particularly in the exploration of compounds with potential therapeutic properties, such as kinase inhibitors or anti-inflammatory agents. Its application is often focused on enabling precise chemical modifications while maintaining stability during synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,390.00 |
+
-
|
| 0.500 | 10-20 days | ฿22,365.00 |
+
-
|
4-nitrobenzyl 2-(((tert-butyldimethylsilyl)oxy)methyl)-6,7-dihydropyrazolo[1,5-a]pyrazine-5(4H)-carboxylate
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry as a protected intermediate. It serves as a key building block in the development of more complex molecules, particularly in the synthesis of biologically active compounds. The tert-butyldimethylsilyl (TBDMS) group acts as a protective moiety for hydroxyl functionalities, ensuring selective reactivity during multi-step synthetic processes. Its nitrobenzyl component can be leveraged in photochemical applications, where it acts as a photolabile protecting group, allowing controlled release of active compounds under specific light conditions. This makes it valuable in the design of prodrugs or targeted drug delivery systems. Additionally, its pyrazolo[1,5-a]pyrazine core structure is of interest in the development of pharmaceuticals, particularly in the exploration of compounds with potential therapeutic properties, such as kinase inhibitors or anti-inflammatory agents. Its application is often focused on enabling precise chemical modifications while maintaining stability during synthesis.
| 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 :