(2S,3R,4S,5S,6R)-6-((Trityloxy)methyl)tetrahydro-2H-pyran-2,3,4,5-tetraol
≥95%
- Product Code: 36535
CAS:
54325-28-9
| Molecular Weight: | 422.47 g./mol | Molecular Formula: | C₂₅H₂₆O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00061632 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily used in organic synthesis as a protected form of a sugar derivative. It serves as an intermediate in the preparation of complex carbohydrates and glycoconjugates. The trityl group acts as a protective moiety for the hydroxyl group, allowing selective reactions to occur at other sites of the molecule. This compound is particularly valuable in the synthesis of oligosaccharides, where precise control over the reactivity of hydroxyl groups is essential. It is also employed in the development of glycosylated pharmaceuticals and bioactive molecules, where the sugar moiety plays a critical role in biological activity. Additionally, it finds application in the study of carbohydrate chemistry and enzymatic processes involving glycosylation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $161.39 |
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| 0.250 | 10-20 days | $242.09 |
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| 1.000 | 10-20 days | $604.87 |
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(2S,3R,4S,5S,6R)-6-((Trityloxy)methyl)tetrahydro-2H-pyran-2,3,4,5-tetraol
This chemical is primarily used in organic synthesis as a protected form of a sugar derivative. It serves as an intermediate in the preparation of complex carbohydrates and glycoconjugates. The trityl group acts as a protective moiety for the hydroxyl group, allowing selective reactions to occur at other sites of the molecule. This compound is particularly valuable in the synthesis of oligosaccharides, where precise control over the reactivity of hydroxyl groups is essential. It is also employed in the development of glycosylated pharmaceuticals and bioactive molecules, where the sugar moiety plays a critical role in biological activity. Additionally, it finds application in the study of carbohydrate chemistry and enzymatic processes involving glycosylation.
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