2-(2-((tert-butyldimethylsilyl)oxy)phenyl)ethanol
95%
- Product Code: 85155
CAS:
160701-56-4
| Molecular Weight: | 252.42 g./mol | Molecular Formula: | C₁₄H₂₄O₂Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31802577 | |
| Melting Point: | Boiling Point: | 304.7±25.0 °C(Predicted) | |
| Density: | 0.963±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized as an intermediate in organic synthesis, particularly in the preparation of more complex molecules. It is often employed in the protection of hydroxyl groups during multi-step synthetic processes, especially in the synthesis of pharmaceuticals and fine chemicals. The tert-butyldimethylsilyl (TBDMS) group serves as a protective group for alcohols, ensuring selective reactions can occur at other sites of the molecule without interference. Additionally, it finds application in the development of bioactive compounds, where the protected alcohol functionality can be later deprotected to reveal the active hydroxyl group. Its use is crucial in maintaining the integrity of sensitive functional groups during complex chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,860.00 |
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| 0.250 | 10-20 days | ฿9,450.00 |
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| 1.000 | 10-20 days | ฿18,900.00 |
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2-(2-((tert-butyldimethylsilyl)oxy)phenyl)ethanol
This chemical is primarily utilized as an intermediate in organic synthesis, particularly in the preparation of more complex molecules. It is often employed in the protection of hydroxyl groups during multi-step synthetic processes, especially in the synthesis of pharmaceuticals and fine chemicals. The tert-butyldimethylsilyl (TBDMS) group serves as a protective group for alcohols, ensuring selective reactions can occur at other sites of the molecule without interference. Additionally, it finds application in the development of bioactive compounds, where the protected alcohol functionality can be later deprotected to reveal the active hydroxyl group. Its use is crucial in maintaining the integrity of sensitive functional groups during complex chemical transformations.
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