(3AR,6R,6aR)-6-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one
97%
- Product Code: 97215
CAS:
75467-36-6
| Molecular Weight: | 302.44 g./mol | Molecular Formula: | C₁₄H₂₆O₅Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00216623 | |
| Melting Point: | 72-74 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily used in organic synthesis as a protected intermediate for the preparation of complex molecules, particularly in the synthesis of nucleosides and carbohydrates. Its structure, featuring a silyl ether protecting group, allows for selective manipulation of functional groups during multi-step reactions. It is often employed in the development of pharmaceuticals, where precise control over stereochemistry is crucial. Additionally, it serves as a key building block in the synthesis of antiviral and anticancer agents, enabling researchers to modify specific regions of the molecule without affecting other sensitive parts. Its stability under various reaction conditions makes it a valuable tool in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,700.00 |
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| 0.250 | 10-20 days | ฿21,060.00 |
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| 1.000 | 10-20 days | ฿42,120.00 |
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(3AR,6R,6aR)-6-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one
This compound is primarily used in organic synthesis as a protected intermediate for the preparation of complex molecules, particularly in the synthesis of nucleosides and carbohydrates. Its structure, featuring a silyl ether protecting group, allows for selective manipulation of functional groups during multi-step reactions. It is often employed in the development of pharmaceuticals, where precise control over stereochemistry is crucial. Additionally, it serves as a key building block in the synthesis of antiviral and anticancer agents, enabling researchers to modify specific regions of the molecule without affecting other sensitive parts. Its stability under various reaction conditions makes it a valuable tool in medicinal chemistry and drug discovery.
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