Phenyl 3,4,6-Tri-O-acetyl-2-deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-β-D-glucopyranoside
≥98%
- Product Code: 103995
CAS:
187022-49-7
| Molecular Weight: | 572.83 g./mol | Molecular Formula: | C₂₁H₂₄Cl₃NO₉S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11112181 | |
| Melting Point: | 143°C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | -20°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the synthesis of glycosyl donors, which are essential for constructing glycosidic bonds in oligosaccharides. The presence of protective groups, such as acetyl and trichloroethoxyformamido, allows for selective deprotection and further functionalization, making it a versatile building block in carbohydrate chemistry. Additionally, its thio-glycoside moiety enhances its stability and reactivity, facilitating its use in glycosylation reactions. This compound is particularly valuable in the development of biologically active molecules, including glycopeptides and glycolipids, which have applications in drug discovery and biochemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $148.65 |
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Phenyl 3,4,6-Tri-O-acetyl-2-deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-β-D-glucopyranoside
This compound is primarily utilized in the field of organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the synthesis of glycosyl donors, which are essential for constructing glycosidic bonds in oligosaccharides. The presence of protective groups, such as acetyl and trichloroethoxyformamido, allows for selective deprotection and further functionalization, making it a versatile building block in carbohydrate chemistry. Additionally, its thio-glycoside moiety enhances its stability and reactivity, facilitating its use in glycosylation reactions. This compound is particularly valuable in the development of biologically active molecules, including glycopeptides and glycolipids, which have applications in drug discovery and biochemical research.
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