2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl Azide
≥98%
- Product Code: 103652
CAS:
53784-29-5
| Molecular Weight: | 373.32 g./mol | Molecular Formula: | C₁₄H₁₉N₃O₉ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05664724 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycosides and glycoconjugates. It serves as a versatile building block in click chemistry reactions, particularly in copper-catalyzed azide-alkyne cycloaddition (CuAAC), to create triazole-linked glycoconjugates. These glycoconjugates are valuable in drug discovery, bioconjugation, and the development of glycopeptides or glycoproteins. Additionally, it is employed in the synthesis of mannose-containing oligosaccharides, which are essential for studying carbohydrate-protein interactions and developing carbohydrate-based vaccines or therapeutics. Its acetylated form provides stability and controlled reactivity, making it suitable for selective glycosylation processes.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Colourless To White To Yellow Solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | Ft22,086.92 |
+
-
|
| 0.250 | 10-20 days | Ft88,670.91 |
+
-
|
2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl Azide
This chemical is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of complex glycosides and glycoconjugates. It serves as a versatile building block in click chemistry reactions, particularly in copper-catalyzed azide-alkyne cycloaddition (CuAAC), to create triazole-linked glycoconjugates. These glycoconjugates are valuable in drug discovery, bioconjugation, and the development of glycopeptides or glycoproteins. Additionally, it is employed in the synthesis of mannose-containing oligosaccharides, which are essential for studying carbohydrate-protein interactions and developing carbohydrate-based vaccines or therapeutics. Its acetylated form provides stability and controlled reactivity, making it suitable for selective glycosylation processes.
| 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:
Ft0.00
Ft0.00
Total :