1,3,4,6-Tetra-O-acetyl-2-[(azidoacetyl)amino]-2-deoxy-β-D-galactopyranos
≥98%
- Product Code: 103629
CAS:
653600-56-7
| Molecular Weight: | 430.13 g./mol | Molecular Formula: | C₁₆H₂₂N₄O₁₀ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized 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 glycosylated molecules, particularly in the development of glycoproteins and glycolipids. The azido group in the molecule allows for efficient click chemistry reactions, enabling the attachment of various functional groups or labels for further study. This makes it valuable in the design of probes for studying carbohydrate-protein interactions, which are crucial in understanding cell signaling and immune responses. Additionally, it is used in the development of vaccines and therapeutic agents targeting specific carbohydrate structures on cell surfaces. Its acetyl groups provide protection during synthetic processes, ensuring the stability and reactivity of the molecule in complex chemical transformations.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White Powder |
| Purity (%) | 98-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿8,220.00 |
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| 0.050 | 10-20 days | ฿27,600.00 |
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1,3,4,6-Tetra-O-acetyl-2-[(azidoacetyl)amino]-2-deoxy-β-D-galactopyranos
This compound is primarily utilized 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 glycosylated molecules, particularly in the development of glycoproteins and glycolipids. The azido group in the molecule allows for efficient click chemistry reactions, enabling the attachment of various functional groups or labels for further study. This makes it valuable in the design of probes for studying carbohydrate-protein interactions, which are crucial in understanding cell signaling and immune responses. Additionally, it is used in the development of vaccines and therapeutic agents targeting specific carbohydrate structures on cell surfaces. Its acetyl groups provide protection during synthetic processes, ensuring the stability and reactivity of the molecule in complex chemical transformations.
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