(4-Bromo-3-Chlorophenoxy)(Tert-Butyl)Dimethylsilane
95%
- Product Code: 150881
CAS:
179120-53-7
| Molecular Weight: | 321.71 g./mol | Molecular Formula: | C₁₂H₁₈BrClOSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28976828 | |
| Melting Point: | Boiling Point: | 297.0±30.0 °C(Predicted) | |
| Density: | 1.237±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature |
Product Description:
Used primarily as a protected intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. The silyl ether group provides stability and selectivity during multi-step reactions, allowing for controlled functional group transformations. Its halogenated aromatic structure makes it valuable in cross-coupling reactions, such as Suzuki or Ullmann couplings, where selective halogen reactivity can be exploited. Commonly employed in the synthesis of complex bioactive molecules where temporary protection of phenolic hydroxyl groups is required. Also utilized in the development of novel pesticides and herbicides due to the enhanced lipophilicity and environmental stability imparted by the silane and halogen substituents.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | Ft119,405.13 |
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| 250mg | 10-20 days | Ft214,867.84 |
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| 1g | 10-20 days | Ft429,735.68 |
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(4-Bromo-3-Chlorophenoxy)(Tert-Butyl)Dimethylsilane
Used primarily as a protected intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. The silyl ether group provides stability and selectivity during multi-step reactions, allowing for controlled functional group transformations. Its halogenated aromatic structure makes it valuable in cross-coupling reactions, such as Suzuki or Ullmann couplings, where selective halogen reactivity can be exploited. Commonly employed in the synthesis of complex bioactive molecules where temporary protection of phenolic hydroxyl groups is required. Also utilized in the development of novel pesticides and herbicides due to the enhanced lipophilicity and environmental stability imparted by the silane and halogen substituents.
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