(2R,3R,4S,5S,6S)-2-(Acetoxymethyl)-6-hydroxytetrahydro-2H-pyran-3,4,5-triyl triacetate
97%
- Product Code: 36482
CAS:
22860-22-6
Molecular Weight: | 348.30 g./mol | Molecular Formula: | C₁₄H₂₀O₁₀ |
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EC Number: | MDL Number: | MFCD08274522 | |
Melting Point: | Boiling Point: | 425.0±45.0°C at 760 mmHg | |
Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a crucial role in carbohydrate chemistry research. It serves as a key intermediate in the preparation of glycosides, which are important for studying biological processes such as cell signaling and immune response. Additionally, it is used in the development of glycopeptides and glycoproteins, which have applications in drug discovery and vaccine development. Its acetylated structure allows for selective deprotection, enabling precise control over glycosylation reactions. This compound is also employed in the production of oligosaccharides, which are essential for understanding carbohydrate-protein interactions and designing therapeutic agents targeting these interactions.
Product Specification:
Test | Specification |
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APPEARANCE | White to light-yellow Solid |
PURITY | 96.5 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,660.00 |
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0.250 | 10-20 days | ฿3,520.00 |
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1.000 | 10-20 days | ฿10,880.00 |
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(2R,3R,4S,5S,6S)-2-(Acetoxymethyl)-6-hydroxytetrahydro-2H-pyran-3,4,5-triyl triacetate
This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, playing a crucial role in carbohydrate chemistry research. It serves as a key intermediate in the preparation of glycosides, which are important for studying biological processes such as cell signaling and immune response. Additionally, it is used in the development of glycopeptides and glycoproteins, which have applications in drug discovery and vaccine development. Its acetylated structure allows for selective deprotection, enabling precise control over glycosylation reactions. This compound is also employed in the production of oligosaccharides, which are essential for understanding carbohydrate-protein interactions and designing therapeutic agents targeting these interactions.
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