(5-Cyanobenzo[b]thiophen-2-yl)boronic acid
95%
- Product Code: 120068
CAS:
1142946-81-3
| Molecular Weight: | 203.03 g./mol | Molecular Formula: | C₉H₆BNO₂S |
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| EC Number: | MDL Number: | MFCD15143421 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, inert gas |
Product Description:
(5-Cyanobenzo[b]thiophen-2-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The boronic acid group in the compound acts as a key functional group, enabling the coupling with various aryl or vinyl halides in the presence of a palladium catalyst. Its application extends to the development of complex organic molecules, including biologically active compounds and organic electronic materials. Additionally, the cyano group on the benzo[b]thiophene ring can enhance the compound's reactivity and provide a handle for further chemical modifications. This makes it a versatile intermediate in medicinal chemistry and material science research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿6,606.00 |
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| 0.100 | 10-20 days | ฿10,557.00 |
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| 0.250 | 10-20 days | ฿15,831.00 |
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(5-Cyanobenzo[b]thiophen-2-yl)boronic acid
(5-Cyanobenzo[b]thiophen-2-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The boronic acid group in the compound acts as a key functional group, enabling the coupling with various aryl or vinyl halides in the presence of a palladium catalyst. Its application extends to the development of complex organic molecules, including biologically active compounds and organic electronic materials. Additionally, the cyano group on the benzo[b]thiophene ring can enhance the compound's reactivity and provide a handle for further chemical modifications. This makes it a versatile intermediate in medicinal chemistry and material science research.
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