(2S,3S,4R,5S,6R)-3-Acetamido-6-(acetoxymethyl)tetrahydro-2H-pyran-2,4,5-triyl triacetate
97%
- Product Code: 237970
CAS:
6730-10-5
| Molecular Weight: | 389.355 g./mol | Molecular Formula: | C₁₆H₂₃NO₁₀ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30491713 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Widely used in the synthesis of sialic acid derivatives, this compound serves as a key glycosyl donor in the preparation of complex carbohydrates and glycoconjugates. Its protected functional groups allow selective deprotection and coupling, making it valuable in the development of pharmaceuticals targeting viral infections, especially influenza, where sialic acid plays a role in receptor binding. It is also employed in the creation of glycan arrays for studying cell-surface interactions and immune responses. Due to its stereochemical purity, it ensures high fidelity in glycosidic bond formation during automated oligosaccharide synthesis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,120.00 |
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| 1g | 10-20 days | ฿8,850.00 |
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| 5g | 10-20 days | ฿37,290.00 |
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| 250mg | 10-20 days | ฿3,290.00 |
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(2S,3S,4R,5S,6R)-3-Acetamido-6-(acetoxymethyl)tetrahydro-2H-pyran-2,4,5-triyl triacetate
Widely used in the synthesis of sialic acid derivatives, this compound serves as a key glycosyl donor in the preparation of complex carbohydrates and glycoconjugates. Its protected functional groups allow selective deprotection and coupling, making it valuable in the development of pharmaceuticals targeting viral infections, especially influenza, where sialic acid plays a role in receptor binding. It is also employed in the creation of glycan arrays for studying cell-surface interactions and immune responses. Due to its stereochemical purity, it ensures high fidelity in glycosidic bond formation during automated oligosaccharide synthesis.
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| Stable in pH range | - |
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