1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-glucopyranose
≥98%
- Product Code: 103620
CAS:
56883-33-1
| Molecular Weight: | 373.32 g./mol | Molecular Formula: | C₁₄H₁₉N₃O₉ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is widely used in carbohydrate chemistry and glycobiology research as a key intermediate for synthesizing complex glycoconjugates. Its azido group allows for selective chemical modifications through click chemistry, particularly in the preparation of glycosyl donors or acceptors. It is instrumental in the synthesis of oligosaccharides, glycopeptides, and glycoproteins, which are essential for studying biological processes like cell signaling and immune responses. Additionally, it serves as a precursor for creating glycosaminoglycan analogs, which are important in drug development and tissue engineering. Its acetyl groups provide protection during synthetic steps, ensuring selective reactivity in multi-step organic transformations.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White Powder |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,980.00 |
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| 0.250 | 10-20 days | ฿5,800.00 |
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| 1.000 | 10-20 days | ฿12,870.00 |
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| 5.000 | 10-20 days | ฿49,880.00 |
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1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-glucopyranose
This compound is widely used in carbohydrate chemistry and glycobiology research as a key intermediate for synthesizing complex glycoconjugates. Its azido group allows for selective chemical modifications through click chemistry, particularly in the preparation of glycosyl donors or acceptors. It is instrumental in the synthesis of oligosaccharides, glycopeptides, and glycoproteins, which are essential for studying biological processes like cell signaling and immune responses. Additionally, it serves as a precursor for creating glycosaminoglycan analogs, which are important in drug development and tissue engineering. Its acetyl groups provide protection during synthetic steps, ensuring selective reactivity in multi-step organic transformations.
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