(3-((3-(Trifluoromethyl)phenyl)carbamoyl)phenyl)boronic acid
98%
- Product Code: 89097
CAS:
882678-73-1
| Molecular Weight: | 309.05 g./mol | Molecular Formula: | C₁₄H₁₁BF₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384304 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates coupling 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 trifluoromethylphenyl moiety enhances its utility in designing compounds with improved stability and bioavailability, often applied in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿18,477.00 |
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(3-((3-(Trifluoromethyl)phenyl)carbamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates coupling 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 trifluoromethylphenyl moiety enhances its utility in designing compounds with improved stability and bioavailability, often applied in drug discovery and development.
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