(3aR,5R,6R,6aR)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol
95%
- Product Code: 84960
CAS:
190970-10-6
| Molecular Weight: | 428.59 g./mol | Molecular Formula: | C₂₄H₃₂O₅Si |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 495.5±45.0 °C(Predicted) | |
| Density: | 1.16±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a protected intermediate for the preparation of complex molecules, particularly in carbohydrate chemistry. Its structure, featuring a tert-butyldiphenylsilyl (TBDPS) protecting group, allows for selective deprotection during multi-step synthetic processes. This makes it valuable in the synthesis of nucleosides, nucleotides, and other biologically active compounds where precise control over hydroxyl group reactivity is required. Additionally, it serves as a key building block in the development of pharmaceuticals, enabling the construction of intricate sugar moieties essential for drug design. Its stability and ease of manipulation under various reaction conditions further enhance its utility in advanced chemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £317.54 |
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| 0.250 | 10-20 days | £582.16 |
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| 1.000 | 10-20 days | £1,164.32 |
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(3aR,5R,6R,6aR)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol
This compound is primarily utilized in organic synthesis as a protected intermediate for the preparation of complex molecules, particularly in carbohydrate chemistry. Its structure, featuring a tert-butyldiphenylsilyl (TBDPS) protecting group, allows for selective deprotection during multi-step synthetic processes. This makes it valuable in the synthesis of nucleosides, nucleotides, and other biologically active compounds where precise control over hydroxyl group reactivity is required. Additionally, it serves as a key building block in the development of pharmaceuticals, enabling the construction of intricate sugar moieties essential for drug design. Its stability and ease of manipulation under various reaction conditions further enhance its utility in advanced chemical research.
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