Allyl-tetra-O-acetyl-β-D-glucopyranoside
98%
- Product Code: 103948
CAS:
10343-15-4
| Molecular Weight: | 388.37 g./mol | Molecular Formula: | C₁₇H₂₄O₁₀ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427087 | |
| Melting Point: | 87-90°C(lit.) | Boiling Point: | 438.6°C at N/A mmHg |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis and carbohydrate chemistry. It serves as a key intermediate in the preparation of complex glycosides and oligosaccharides, which are essential in the study of glycobiology and the development of glycoconjugate vaccines. Its acetyl-protected hydroxyl groups make it a valuable building block for selective glycosylation reactions, enabling the creation of specific glycosidic linkages. Additionally, it is employed in the synthesis of bioactive molecules and natural products, where precise control over sugar moiety attachment is crucial. Its stability and reactivity under controlled conditions make it a preferred choice for researchers working on carbohydrate-based drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,053.00 |
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| 0.500 | 10-20 days | ฿3,681.00 |
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Allyl-tetra-O-acetyl-β-D-glucopyranoside
This compound is primarily utilized in the field of organic synthesis and carbohydrate chemistry. It serves as a key intermediate in the preparation of complex glycosides and oligosaccharides, which are essential in the study of glycobiology and the development of glycoconjugate vaccines. Its acetyl-protected hydroxyl groups make it a valuable building block for selective glycosylation reactions, enabling the creation of specific glycosidic linkages. Additionally, it is employed in the synthesis of bioactive molecules and natural products, where precise control over sugar moiety attachment is crucial. Its stability and reactivity under controlled conditions make it a preferred choice for researchers working on carbohydrate-based drug discovery and development.
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