Methyl 2,3,4,6-tetra-O-benzyl-a-D-galactopyranoside
98%
- Product Code: 103954
CAS:
53008-63-2
| Molecular Weight: | 554.65 g./mol | Molecular Formula: | C₃₅H₃₈O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09756157 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosides and oligosaccharides, which are crucial in biochemical and pharmaceutical research. The compound is particularly valuable in the study of carbohydrate-protein interactions, aiding in the development of glycobiology-based therapeutics. Additionally, it is employed in the synthesis of glycosyl donors, which are essential for constructing specific glycosidic linkages in carbohydrate chemistry. Its benzyl-protected groups provide stability during synthetic processes, making it a versatile reagent in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft38,786.79 |
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Methyl 2,3,4,6-tetra-O-benzyl-a-D-galactopyranoside
This chemical is primarily used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of glycosides and oligosaccharides, which are crucial in biochemical and pharmaceutical research. The compound is particularly valuable in the study of carbohydrate-protein interactions, aiding in the development of glycobiology-based therapeutics. Additionally, it is employed in the synthesis of glycosyl donors, which are essential for constructing specific glycosidic linkages in carbohydrate chemistry. Its benzyl-protected groups provide stability during synthetic processes, making it a versatile reagent in organic synthesis.
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