(2-Bromoethoxy)-tert-butyldimethylsilane
96%
- Product Code: 87991
CAS:
86864-60-0
| Molecular Weight: | 239.23 g./mol | Molecular Formula: | BrCH₂CH₂OSiCH₃₂CCH₃₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00209550 | |
| Melting Point: | Boiling Point: | 70-75 °C2.5 mm Hg(lit.) | |
| Density: | 1.115 g/mL at 25 °C(lit.) | Storage Condition: | 2~8℃, sealed, protected from light |
Product Description:
This chemical is primarily used as a protecting group reagent in organic synthesis, particularly for alcohols. The tert-butyldimethylsilyl (TBDMS) group is introduced to protect hydroxyl groups during multi-step reactions, ensuring they remain unaffected by subsequent chemical transformations. The bromoethoxy moiety allows for further functionalization or deprotection under mild conditions. It is commonly applied in the synthesis of complex molecules, such as pharmaceuticals, natural products, and polymers, where selective protection and deprotection of functional groups are critical. Its stability under various reaction conditions makes it a valuable tool in synthetic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 95.5-100 |
| APPEARANCE | COLORLESS LIQUID |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿450.00 |
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| 25.000 | 10-20 days | ฿1,900.00 |
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| 100.000 | 10-20 days | ฿7,500.00 |
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(2-Bromoethoxy)-tert-butyldimethylsilane
This chemical is primarily used as a protecting group reagent in organic synthesis, particularly for alcohols. The tert-butyldimethylsilyl (TBDMS) group is introduced to protect hydroxyl groups during multi-step reactions, ensuring they remain unaffected by subsequent chemical transformations. The bromoethoxy moiety allows for further functionalization or deprotection under mild conditions. It is commonly applied in the synthesis of complex molecules, such as pharmaceuticals, natural products, and polymers, where selective protection and deprotection of functional groups are critical. Its stability under various reaction conditions makes it a valuable tool in synthetic chemistry.
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