(4-(Bromomethyl)phenoxy)(tert-butyl)dimethylsilane
95%
- Product Code: 152228
CAS:
120506-39-0
| Molecular Weight: | 301.29 g./mol | Molecular Formula: | C₁₃H₂₁BrOSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27920682 | |
| Melting Point: | Boiling Point: | 291.5±23.0 °C(Predicted) | |
| Density: | 1.153±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, inert gas |
Product Description:
Used primarily as a silyl protecting group reagent in organic synthesis, particularly in the protection of phenolic hydroxyl groups during multi-step reactions. The compound allows selective protection due to the stability of the silyl ether formed, which can be removed under mild conditions without affecting other functional groups. Its (bromomethyl)phenoxy moiety provides a handle for further functionalization or anchoring to solid supports in combinatorial chemistry and drug discovery. Commonly employed in the synthesis of complex natural products and pharmaceuticals where controlled deprotection and high yields are critical.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,520.00 |
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| 1.000 | 10-20 days | ฿9,470.00 |
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| 5.000 | 10-20 days | ฿38,630.00 |
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(4-(Bromomethyl)phenoxy)(tert-butyl)dimethylsilane
Used primarily as a silyl protecting group reagent in organic synthesis, particularly in the protection of phenolic hydroxyl groups during multi-step reactions. The compound allows selective protection due to the stability of the silyl ether formed, which can be removed under mild conditions without affecting other functional groups. Its (bromomethyl)phenoxy moiety provides a handle for further functionalization or anchoring to solid supports in combinatorial chemistry and drug discovery. Commonly employed in the synthesis of complex natural products and pharmaceuticals where controlled deprotection and high yields are critical.
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