Phenyl 2,3,4,6-Tetra-O-benzyl-1-thio-β-D-galactopyranoside
≥98%
- Product Code: 103999
CAS:
74801-29-9
| Molecular Weight: | 632.8200000000001 g./mol | Molecular Formula: | C₄₀H₄₀O₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06657856 | |
| Melting Point: | 86-90°C | Boiling Point: | |
| Density: | Storage Condition: | -20°C |
Product Description:
Phenyl 2,3,4,6-Tetra-O-benzyl-1-thio-β-D-galactopyranoside is primarily used in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates. The compound is particularly valuable in the preparation of glycosyl donors, which are essential for constructing glycosidic linkages in a controlled and stereospecific manner. Its benzyl-protected groups ensure stability during synthetic processes, while the thio moiety enhances reactivity in glycosylation reactions. This chemical is widely employed in the development of glycosylated natural products, glycoproteins, and other biologically relevant molecules for studies in drug discovery, immunology, and enzymatic activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €94.50 |
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Phenyl 2,3,4,6-Tetra-O-benzyl-1-thio-β-D-galactopyranoside
Phenyl 2,3,4,6-Tetra-O-benzyl-1-thio-β-D-galactopyranoside is primarily used in carbohydrate chemistry and glycobiology research. It serves as a key intermediate in the synthesis of complex oligosaccharides and glycoconjugates. The compound is particularly valuable in the preparation of glycosyl donors, which are essential for constructing glycosidic linkages in a controlled and stereospecific manner. Its benzyl-protected groups ensure stability during synthetic processes, while the thio moiety enhances reactivity in glycosylation reactions. This chemical is widely employed in the development of glycosylated natural products, glycoproteins, and other biologically relevant molecules for studies in drug discovery, immunology, and enzymatic activity.
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