3,5-Bis(tert-butyldiphenylsilyloxy)benzyl Alcohol
95%
- Product Code: 94517
CAS:
182250-70-0
| Molecular Weight: | 616.95 g./mol | Molecular Formula: | C₃₉H₄₄O₃Si₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02093440 | |
| Melting Point: | 106.0-111.0°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a protecting group for alcohols. Its bulky tert-butyldiphenylsilyl groups provide steric hindrance, making it effective in selectively protecting hydroxyl groups during complex multi-step reactions. This is particularly useful in the synthesis of natural products, pharmaceuticals, and fine chemicals, where precise control over reactivity is essential. Additionally, its stability under various reaction conditions allows it to be used in transformations involving acidic or basic environments. After the desired reactions are completed, the protecting groups can be removed under mild conditions, restoring the free alcohol functionality without damaging the molecule.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿2,000.00 |
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| 1.000 | 10-20 days | ฿7,600.00 |
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3,5-Bis(tert-butyldiphenylsilyloxy)benzyl Alcohol
This chemical is primarily utilized in organic synthesis as a protecting group for alcohols. Its bulky tert-butyldiphenylsilyl groups provide steric hindrance, making it effective in selectively protecting hydroxyl groups during complex multi-step reactions. This is particularly useful in the synthesis of natural products, pharmaceuticals, and fine chemicals, where precise control over reactivity is essential. Additionally, its stability under various reaction conditions allows it to be used in transformations involving acidic or basic environments. After the desired reactions are completed, the protecting groups can be removed under mild conditions, restoring the free alcohol functionality without damaging the molecule.
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