3-O-Benzyl-1,2:5,6-bis-O-isopropylidene-alpha-D-galactofuranose
98%
- Product Code: 103711
CAS:
22331-21-1
| Molecular Weight: | 350.406 g./mol | Molecular Formula: | C₁₉H₂₆O₆ |
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| EC Number: | MDL Number: | MFCD08704028 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a protected intermediate in the synthesis of galactofuranose-containing molecules, which are significant in the study of glycobiology and the development of bioactive compounds. The benzyl and isopropylidene groups act as protective moieties, allowing selective manipulation of the sugar molecule during synthetic processes. This compound is especially valuable in the production of oligosaccharides and glycoproteins, which have applications in drug development, vaccine design, and the study of cellular recognition processes. Its role in facilitating the construction of structurally intricate carbohydrates makes it a key reagent in carbohydrate chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿9,650.00 |
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3-O-Benzyl-1,2:5,6-bis-O-isopropylidene-alpha-D-galactofuranose
This chemical is primarily utilized in organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a protected intermediate in the synthesis of galactofuranose-containing molecules, which are significant in the study of glycobiology and the development of bioactive compounds. The benzyl and isopropylidene groups act as protective moieties, allowing selective manipulation of the sugar molecule during synthetic processes. This compound is especially valuable in the production of oligosaccharides and glycoproteins, which have applications in drug development, vaccine design, and the study of cellular recognition processes. Its role in facilitating the construction of structurally intricate carbohydrates makes it a key reagent in carbohydrate chemistry research.
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