2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl p-Trifluoromethylbenzylthio-N-(p-trifluoromethylphenyl)formimidate
≥95%
- Product Code: 103659
CAS:
468095-63-8
| Molecular Weight: | 901.96 g./mol | Molecular Formula: | C₅₀H₄₅F₆NO₆S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06797177 | |
| Melting Point: | 120-125°C | Boiling Point: | |
| Density: | Storage Condition: | -20°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrate derivatives. It serves as a key intermediate in glycosylation reactions, enabling the formation of glycosidic bonds with high selectivity and efficiency. Its application is significant in the development of glycoconjugates, which are essential in the study of biological processes and the design of carbohydrate-based drugs. Additionally, it is employed in the synthesis of glycosyl donors, which are crucial for constructing oligosaccharides and polysaccharides with specific structural features. Its use extends to research in glycobiology, where it aids in understanding the role of carbohydrates in cellular interactions and signaling pathways. The compound’s stability and reactivity make it a valuable tool in the synthesis of biologically active molecules and potential therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿5,454.00 |
+
-
|
2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl p-Trifluoromethylbenzylthio-N-(p-trifluoromethylphenyl)formimidate
This compound is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrate derivatives. It serves as a key intermediate in glycosylation reactions, enabling the formation of glycosidic bonds with high selectivity and efficiency. Its application is significant in the development of glycoconjugates, which are essential in the study of biological processes and the design of carbohydrate-based drugs. Additionally, it is employed in the synthesis of glycosyl donors, which are crucial for constructing oligosaccharides and polysaccharides with specific structural features. Its use extends to research in glycobiology, where it aids in understanding the role of carbohydrates in cellular interactions and signaling pathways. The compound’s stability and reactivity make it a valuable tool in the synthesis of biologically active molecules and potential therapeutic agents.
| 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 :