(2R,3R,4S,5S,6R)-2-(Acetoxymethyl)-6-(2,2,2-trichloro-1-iminoethoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
95%
- Product Code: 87064
CAS:
121238-27-5
| Molecular Weight: | 492.69 g./mol | Molecular Formula: | C₁₆H₂₀Cl₃NO₁₀ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04039685 | |
| Melting Point: | 62-64 °C | Boiling Point: | 463.3±55.0 °C(Predicted) |
| Density: | 1.55±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of complex carbohydrates and glycoconjugates. Its structure, featuring multiple acetate groups and a trichloroethoxy moiety, makes it a valuable building block for constructing glycosidic linkages in carbohydrate chemistry. It is often employed in the synthesis of oligosaccharides and glycoproteins, which are essential for research in biochemistry and medicinal chemistry. Additionally, its reactivity allows for selective modifications, enabling the creation of tailored molecules for drug development and biological studies. Its role in advancing glycobiology and the development of carbohydrate-based therapeutics highlights its importance in modern chemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | £80.20 |
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| 1.000 | 10-20 days | £216.17 |
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| 5.000 | 10-20 days | £756.20 |
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(2R,3R,4S,5S,6R)-2-(Acetoxymethyl)-6-(2,2,2-trichloro-1-iminoethoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate
This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of complex carbohydrates and glycoconjugates. Its structure, featuring multiple acetate groups and a trichloroethoxy moiety, makes it a valuable building block for constructing glycosidic linkages in carbohydrate chemistry. It is often employed in the synthesis of oligosaccharides and glycoproteins, which are essential for research in biochemistry and medicinal chemistry. Additionally, its reactivity allows for selective modifications, enabling the creation of tailored molecules for drug development and biological studies. Its role in advancing glycobiology and the development of carbohydrate-based therapeutics highlights its importance in modern chemical research.
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