(5-Cyanothiophen-2-yl)boronic acid
97%
- Product Code: 90901
CAS:
305832-67-1
| Molecular Weight: | 152.97 g./mol | Molecular Formula: | C₅H₄BNO₂S |
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| Melting Point: | 175°C | Boiling Point: | 369.3°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
(5-Cyanothiophen-2-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in the synthesis of biologically active compounds. Additionally, it is utilized in the development of organic electronic materials, such as polymers and small molecules, for applications in optoelectronics and sensors. Its versatility and reactivity make it a crucial component in modern synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿378.00 |
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| 1.000 | 10-20 days | ฿945.00 |
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(5-Cyanothiophen-2-yl)boronic acid
(5-Cyanothiophen-2-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in the synthesis of biologically active compounds. Additionally, it is utilized in the development of organic electronic materials, such as polymers and small molecules, for applications in optoelectronics and sensors. Its versatility and reactivity make it a crucial component in modern synthetic chemistry.
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