2-Azidoethyl 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranoside
≥92%
- Product Code: 103687
CAS:
140428-81-5
| Molecular Weight: | 417.37 g./mol | Molecular Formula: | C₁₆H₂₃N₃O₁₀ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates, which are essential in biochemical and pharmaceutical research. It serves as a key intermediate in the preparation of glycosyl azides, which are valuable for click chemistry reactions, particularly the copper-catalyzed azide-alkyne cycloaddition (CuAAC). This reaction is widely employed in bioconjugation, labeling, and the development of bioactive molecules, including drug candidates and diagnostic probes. Additionally, its acetyl-protected glucose moiety makes it suitable for selective deprotection and further functionalization, enabling the creation of tailored carbohydrate structures for studying biological processes or designing glycotherapeutics.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Almost White Powder To Crystal |
| Purity (%) | 91.5-100 |
| Specific Rotation [A]20/D(C=1.5, CHCl3) | -40.0--33.0 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿4,680.00 |
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| 1.000 | 10-20 days | ฿17,440.00 |
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2-Azidoethyl 2,3,4,6-Tetra-O-acetyl-β-D-glucopyranoside
This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates, which are essential in biochemical and pharmaceutical research. It serves as a key intermediate in the preparation of glycosyl azides, which are valuable for click chemistry reactions, particularly the copper-catalyzed azide-alkyne cycloaddition (CuAAC). This reaction is widely employed in bioconjugation, labeling, and the development of bioactive molecules, including drug candidates and diagnostic probes. Additionally, its acetyl-protected glucose moiety makes it suitable for selective deprotection and further functionalization, enabling the creation of tailored carbohydrate structures for studying biological processes or designing glycotherapeutics.
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