5-(2-Trifluoromethylphenyl)thiophene-2-boronic acid
95%
- Product Code: 92240
CAS:
2225177-18-2
| Molecular Weight: | 272.0512296 g./mol | Molecular Formula: | C₁₁H₈BF₃O₂S |
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| Density: | Storage Condition: | -20℃ |
Product Description:
This chemical is widely used in the field of organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. Additionally, the trifluoromethyl group enhances the chemical's stability and influences the electronic properties of the resulting compounds, which is beneficial in drug discovery and material science. Its applications also extend to the development of organic electronics and optoelectronic devices due to its ability to modify molecular structures for desired properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿12,402.00 |
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| 0.100 | 10-20 days | ฿44,892.00 |
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5-(2-Trifluoromethylphenyl)thiophene-2-boronic acid
This chemical is widely used in the field of organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds. Additionally, the trifluoromethyl group enhances the chemical's stability and influences the electronic properties of the resulting compounds, which is beneficial in drug discovery and material science. Its applications also extend to the development of organic electronics and optoelectronic devices due to its ability to modify molecular structures for desired properties.
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