tert-butyldimethyl(4-(prop-1-en-2-yl)phenoxy)silane
98%
- Product Code: 242178
CAS:
129181-43-7
| Molecular Weight: | 248.44 g./mol | Molecular Formula: | C₁₅H₂₄OSi |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
Used as a silyl protecting agent in organic synthesis, particularly for phenolic hydroxyl groups. Its bulky structure provides high selectivity and stability under various reaction conditions, making it valuable in multi-step synthesis of complex molecules such as natural products and pharmaceuticals. The tert-butyldimethylsilyl (TBDMS) group can be introduced selectively and removed under mild conditions, allowing for precise control in the construction of sensitive intermediates. The presence of the prop-1-en-2-yl (isopropenyl) aromatic moiety may also enable further functionalization or act as a directing group in certain transformations. Commonly employed in the synthesis of steroids, prostaglandins, and other bioactive compounds where protection of phenolic OH is required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿6,210.00 |
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| 5.000 | 10-20 days | ฿23,290.00 |
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tert-butyldimethyl(4-(prop-1-en-2-yl)phenoxy)silane
Used as a silyl protecting agent in organic synthesis, particularly for phenolic hydroxyl groups. Its bulky structure provides high selectivity and stability under various reaction conditions, making it valuable in multi-step synthesis of complex molecules such as natural products and pharmaceuticals. The tert-butyldimethylsilyl (TBDMS) group can be introduced selectively and removed under mild conditions, allowing for precise control in the construction of sensitive intermediates. The presence of the prop-1-en-2-yl (isopropenyl) aromatic moiety may also enable further functionalization or act as a directing group in certain transformations. Commonly employed in the synthesis of steroids, prostaglandins, and other bioactive compounds where protection of phenolic OH is required.
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