((5R,6S,6aR)-6-(benzyloxy)-5-((benzyloxy)methyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol
95%
- Product Code: 84757
CAS:
206055-83-6
| Molecular Weight: | 400.46 g./mol | Molecular Formula: | C₂₃H₂₈O₆ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 531.4±50.0 °C(Predicted) | |
| Density: | 1.22±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the field of medicinal chemistry. Its structure, featuring multiple protective groups like benzyloxy and tetrahydrofuro[2,3-d][1,3]dioxol, makes it a valuable intermediate in the preparation of nucleoside analogs. These analogs are crucial in the development of antiviral and anticancer drugs, where they act by inhibiting the replication of DNA or RNA in target cells. Additionally, the compound's stereochemistry and functional groups allow for precise modifications, enabling researchers to tailor its properties for specific therapeutic applications. Its role in carbohydrate chemistry is also notable, as it aids in the construction of glycosidic linkages, which are essential in the synthesis of oligosaccharides and glycoconjugates used in drug discovery and biochemical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,190.00 |
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| 0.250 | 10-20 days | ฿14,625.00 |
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| 1.000 | 10-20 days | ฿29,250.00 |
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((5R,6S,6aR)-6-(benzyloxy)-5-((benzyloxy)methyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the field of medicinal chemistry. Its structure, featuring multiple protective groups like benzyloxy and tetrahydrofuro[2,3-d][1,3]dioxol, makes it a valuable intermediate in the preparation of nucleoside analogs. These analogs are crucial in the development of antiviral and anticancer drugs, where they act by inhibiting the replication of DNA or RNA in target cells. Additionally, the compound's stereochemistry and functional groups allow for precise modifications, enabling researchers to tailor its properties for specific therapeutic applications. Its role in carbohydrate chemistry is also notable, as it aids in the construction of glycosidic linkages, which are essential in the synthesis of oligosaccharides and glycoconjugates used in drug discovery and biochemical studies.
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