methyl 6-O-benzoyl-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside
98%
- Product Code: 54258
CAS:
87907-36-6
| Molecular Weight: | 521.55 g./mol | Molecular Formula: | C₂₉H₃₁NO₈ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the preparation of complex carbohydrate derivatives. It serves as a key intermediate in the synthesis of glycosylated compounds, which are essential in the development of pharmaceuticals, especially in the design of drugs targeting bacterial infections and cancer. The protective groups attached to the molecule, such as benzoyl and benzyl, allow for selective manipulation of specific hydroxyl groups, enabling the construction of highly specific and structurally diverse carbohydrate-based molecules. Additionally, it is employed in the study of enzymatic reactions involving glycosidases and glycosyltransferases, aiding in the understanding of carbohydrate metabolism and the development of enzyme inhibitors.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white or off-white solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿8,270.00 |
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| 5.000 | 10-20 days | ฿24,800.00 |
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methyl 6-O-benzoyl-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside
This chemical is primarily utilized in the field of organic synthesis, particularly in the preparation of complex carbohydrate derivatives. It serves as a key intermediate in the synthesis of glycosylated compounds, which are essential in the development of pharmaceuticals, especially in the design of drugs targeting bacterial infections and cancer. The protective groups attached to the molecule, such as benzoyl and benzyl, allow for selective manipulation of specific hydroxyl groups, enabling the construction of highly specific and structurally diverse carbohydrate-based molecules. Additionally, it is employed in the study of enzymatic reactions involving glycosidases and glycosyltransferases, aiding in the understanding of carbohydrate metabolism and the development of enzyme inhibitors.
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