1-Bromo-3-(trimethylsilyl)benzene
96%
- Product Code: 88145
CAS:
17878-47-6
| Molecular Weight: | 229.19 g./mol | Molecular Formula: | C₉H₁₃BrSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00093882 | |
| Melting Point: | Boiling Point: | 50°C/0.5mmHg(lit.) | |
| Density: | 1.22g/ml | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in organic synthesis as a versatile intermediate. It serves as a building block in the preparation of more complex organic compounds, particularly in the field of pharmaceuticals and materials science. The trimethylsilyl group acts as a protective group for sensitive functional groups during chemical reactions, allowing for selective transformations. Additionally, it is employed in cross-coupling reactions, such as Suzuki-Miyaura and Stille couplings, to create carbon-carbon bonds, which are essential in the synthesis of various organic molecules. Its bromine substituent makes it a suitable candidate for further functionalization through substitution reactions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow Powder or Crystals |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿830.00 |
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| 5.000 | 10-20 days | ฿2,440.00 |
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1-Bromo-3-(trimethylsilyl)benzene
This chemical is primarily used in organic synthesis as a versatile intermediate. It serves as a building block in the preparation of more complex organic compounds, particularly in the field of pharmaceuticals and materials science. The trimethylsilyl group acts as a protective group for sensitive functional groups during chemical reactions, allowing for selective transformations. Additionally, it is employed in cross-coupling reactions, such as Suzuki-Miyaura and Stille couplings, to create carbon-carbon bonds, which are essential in the synthesis of various organic molecules. Its bromine substituent makes it a suitable candidate for further functionalization through substitution reactions.
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