5-[(2R,3R,4R,5R,6R)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-acetamidooxan-2-yl]oxypentanoic acid
97%
- Product Code: 104616
CAS:
1159408-54-4
| Molecular Weight: | 447.43 g./mol | Molecular Formula: | C₁₉H₂₉NO₁₁ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30802159 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20℃, inert gas storage |
Product Description:
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex carbohydrate-based molecules, which are essential for creating glycoconjugates and glycoproteins. These molecules play a critical role in studying biological processes such as cell signaling, immune response, and pathogen recognition. Additionally, it is used in the synthesis of novel drug candidates, particularly those targeting infectious diseases and cancer, due to its structural similarity to natural glycosides. Its acetylated sugar moiety makes it valuable for protecting group strategies in carbohydrate chemistry, enabling precise control over synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.025 | 10-20 days | £94.25 |
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| 0.050 | 10-20 days | £133.33 |
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| 0.100 | 10-20 days | £188.49 |
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5-[(2R,3R,4R,5R,6R)-4,5-bis(acetyloxy)-6-[(acetyloxy)methyl]-3-acetamidooxan-2-yl]oxypentanoic acid
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex carbohydrate-based molecules, which are essential for creating glycoconjugates and glycoproteins. These molecules play a critical role in studying biological processes such as cell signaling, immune response, and pathogen recognition. Additionally, it is used in the synthesis of novel drug candidates, particularly those targeting infectious diseases and cancer, due to its structural similarity to natural glycosides. Its acetylated sugar moiety makes it valuable for protecting group strategies in carbohydrate chemistry, enabling precise control over synthetic pathways.
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