(2-Bromophenylethynyl)trimethylsilane
≥98%
- Product Code: 87993
CAS:
38274-16-7
| Molecular Weight: | 253.21 g./mol | Molecular Formula: | C₁₁H₁₃BrSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01321391 | |
| Melting Point: | Boiling Point: | 91°C/2mmHg(lit.) | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the construction of complex molecular structures. It is often employed in cross-coupling reactions, such as Sonogashira coupling, to introduce alkynyl groups into aromatic systems, which is valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The trimethylsilyl group acts as a protective moiety, enhancing stability and facilitating selective transformations. Additionally, its bromo substituent makes it a useful intermediate for further functionalization via metal-catalyzed reactions. This compound is particularly significant in the synthesis of conjugated polymers and organic semiconductors, where precise control over molecular architecture is critical for optimizing electronic properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to Brown clear liquid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿530.00 |
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| 1.000 | 10-20 days | ฿1,990.00 |
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| 5.000 | 10-20 days | ฿9,620.00 |
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(2-Bromophenylethynyl)trimethylsilane
This chemical is primarily utilized in organic synthesis as a versatile building block for the construction of complex molecular structures. It is often employed in cross-coupling reactions, such as Sonogashira coupling, to introduce alkynyl groups into aromatic systems, which is valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The trimethylsilyl group acts as a protective moiety, enhancing stability and facilitating selective transformations. Additionally, its bromo substituent makes it a useful intermediate for further functionalization via metal-catalyzed reactions. This compound is particularly significant in the synthesis of conjugated polymers and organic semiconductors, where precise control over molecular architecture is critical for optimizing electronic properties.
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