(2-(thiophen-2-yl)pyrimidin-5-yl)boronic acid
95%
- Product Code: 56364
CAS:
2225172-17-6
| Molecular Weight: | 206.02938 g./mol | Molecular Formula: | C₈H₇BN₂O₂S |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid group reacts efficiently with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thiophene and pyrimidine moieties contribute to its utility in designing compounds with potential biological activity, such as drug candidates targeting various diseases. Its role in material science is also notable, as it aids in the development of organic electronic components like OLEDs and semiconductors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿14,260.00 |
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| 0.025 | 10-20 days | ฿49,200.00 |
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| 0.100 | 10-20 days | ฿127,400.00 |
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(2-(thiophen-2-yl)pyrimidin-5-yl)boronic acid
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid group reacts efficiently with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thiophene and pyrimidine moieties contribute to its utility in designing compounds with potential biological activity, such as drug candidates targeting various diseases. Its role in material science is also notable, as it aids in the development of organic electronic components like OLEDs and semiconductors.
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