2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate
98%
- Product Code: 103661
Alias:
2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidic acid
CAS:
74808-09-6
| Molecular Weight: | 685 g./mol | Molecular Formula: | C₃₆H₃₆Cl₃NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03427010 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a glycosyl donor in carbohydrate chemistry. It plays a crucial role in the formation of glycosidic bonds, enabling the construction of complex oligosaccharides and glycoconjugates. Its application is particularly significant in the synthesis of biologically active molecules, such as glycoproteins, glycolipids, and other glycosylated natural products. The trichloroacetimidate group enhances reactivity, making it a preferred choice for stereoselective glycosylation reactions. It is widely employed in pharmaceutical research for the development of carbohydrate-based drugs and vaccines, as well as in biochemical studies to investigate glycosylation processes and their biological functions.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White Crystalline Powder |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿9,200.00 |
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2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate
This chemical is primarily utilized in organic synthesis as a glycosyl donor in carbohydrate chemistry. It plays a crucial role in the formation of glycosidic bonds, enabling the construction of complex oligosaccharides and glycoconjugates. Its application is particularly significant in the synthesis of biologically active molecules, such as glycoproteins, glycolipids, and other glycosylated natural products. The trichloroacetimidate group enhances reactivity, making it a preferred choice for stereoselective glycosylation reactions. It is widely employed in pharmaceutical research for the development of carbohydrate-based drugs and vaccines, as well as in biochemical studies to investigate glycosylation processes and their biological functions.
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