Ethyl 4-((tert-butyldimethylsilyl)oxy)benzoate
95%
- Product Code: 83761
CAS:
153025-65-1
| Molecular Weight: | 280.43 g./mol | Molecular Formula: | C₁₅H₂₄O₃Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08693139 | |
| Melting Point: | Boiling Point: | 313.7±25.0 °C(Predicted) | |
| Density: | 0.979±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis as a protecting group for hydroxyl functionalities, particularly in the preparation of complex molecules. Its tert-butyldimethylsilyl (TBDMS) group shields the hydroxyl group during reactions, allowing selective modification of other parts of the molecule without interference. It is commonly employed in the synthesis of pharmaceuticals, natural products, and fine chemicals, where precise control over reactivity is essential. After the desired reactions are complete, the TBDMS group can be easily removed under mild conditions, restoring the hydroxyl functionality. This makes it a valuable tool in multi-step synthetic processes, particularly in the development of drugs and bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,455.00 |
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| 0.250 | 10-20 days | ฿8,100.00 |
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| 1.000 | 10-20 days | ฿16,200.00 |
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Ethyl 4-((tert-butyldimethylsilyl)oxy)benzoate
This compound is primarily used in organic synthesis as a protecting group for hydroxyl functionalities, particularly in the preparation of complex molecules. Its tert-butyldimethylsilyl (TBDMS) group shields the hydroxyl group during reactions, allowing selective modification of other parts of the molecule without interference. It is commonly employed in the synthesis of pharmaceuticals, natural products, and fine chemicals, where precise control over reactivity is essential. After the desired reactions are complete, the TBDMS group can be easily removed under mild conditions, restoring the hydroxyl functionality. This makes it a valuable tool in multi-step synthetic processes, particularly in the development of drugs and bioactive compounds.
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