(R)-2-((tert-Butyldimethylsilyl)oxy)propan-1-ol
95%
- Product Code: 123673
CAS:
265309-82-8
| Molecular Weight: | 190.36 g./mol | Molecular Formula: | C₉H₂₂O₂Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28401351 | |
| Melting Point: | Boiling Point: | 202.6±23.0 °C(Predicted) | |
| Density: | 0.876±0.06 g/cm3(Predicted) | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily used in organic synthesis as a chiral building block or intermediate. Its tert-butyldimethylsilyl (TBDMS) protecting group is particularly valuable in multi-step synthesis processes, where it safeguards the hydroxyl group from unwanted reactions. The chiral nature of the molecule makes it useful in the production of enantiomerically pure pharmaceuticals, agrochemicals, and fine chemicals. It is often employed in the synthesis of complex natural products or bioactive compounds, where precise stereochemistry is critical. Additionally, the TBDMS group can be selectively removed under mild conditions, allowing for further functionalization of the molecule in subsequent synthetic steps.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿8,253.00 |
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| 0.100 | 10-20 days | ฿13,167.00 |
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| 0.250 | 10-20 days | ฿22,383.00 |
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(R)-2-((tert-Butyldimethylsilyl)oxy)propan-1-ol
This compound is primarily used in organic synthesis as a chiral building block or intermediate. Its tert-butyldimethylsilyl (TBDMS) protecting group is particularly valuable in multi-step synthesis processes, where it safeguards the hydroxyl group from unwanted reactions. The chiral nature of the molecule makes it useful in the production of enantiomerically pure pharmaceuticals, agrochemicals, and fine chemicals. It is often employed in the synthesis of complex natural products or bioactive compounds, where precise stereochemistry is critical. Additionally, the TBDMS group can be selectively removed under mild conditions, allowing for further functionalization of the molecule in subsequent synthetic steps.
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