(2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(benzyloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
95%
- Product Code: 87063
CAS:
10343-13-2
Molecular Weight: | 438.43 g./mol | Molecular Formula: | C₂₁H₂₆O₁₀ |
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EC Number: | MDL Number: | MFCD00184641 | |
Melting Point: | 92-94 °C | Boiling Point: | 499 °C(Predicted) |
Density: | 1.27 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, serving as a key intermediate in the production of oligosaccharides. Its structure allows for selective deprotection and functionalization, making it valuable in glycosylation reactions. It is often employed in the development of glycoproteins and glycolipids, which are crucial in biological research and drug development. Additionally, it plays a role in the study of glycosidase enzymes and their inhibitors, contributing to advancements in the treatment of metabolic disorders and infectious diseases. Its application extends to the preparation of glycosyl donors, which are essential in carbohydrate chemistry for constructing biologically active molecules.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $77.23 |
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0.250 | 10-20 days | $142.84 |
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1.000 | 10-20 days | $432.04 |
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(2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(benzyloxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
This compound is primarily utilized in the synthesis of complex carbohydrates and glycoconjugates, serving as a key intermediate in the production of oligosaccharides. Its structure allows for selective deprotection and functionalization, making it valuable in glycosylation reactions. It is often employed in the development of glycoproteins and glycolipids, which are crucial in biological research and drug development. Additionally, it plays a role in the study of glycosidase enzymes and their inhibitors, contributing to advancements in the treatment of metabolic disorders and infectious diseases. Its application extends to the preparation of glycosyl donors, which are essential in carbohydrate chemistry for constructing biologically active molecules.
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