(1-(Thiophen-3-yl)-1H-pyrazol-4-yl)boronic acid
95%
- Product Code: 88978
CAS:
1974329-41-3
| Molecular Weight: | 194.02 g./mol | Molecular Formula: | C₇H₇BN₂O₂S |
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| EC Number: | MDL Number: | MFCD21099655 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid functional group allows it to react with various aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thiophene and pyrazole moieties contribute to its potential use in designing molecules with specific electronic or biological properties, such as in drug discovery for targeting specific enzymes or receptors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿8,982.00 |
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| 0.025 | 10-20 days | ฿19,800.00 |
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(1-(Thiophen-3-yl)-1H-pyrazol-4-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid functional group allows it to react with various aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thiophene and pyrazole moieties contribute to its potential use in designing molecules with specific electronic or biological properties, such as in drug discovery for targeting specific enzymes or receptors.
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