(4-((2,2,2-Trifluoroethyl)carbamoyl)phenyl)boronic acid
98%
- Product Code: 243593
CAS:
874459-90-2
| Molecular Weight: | 246.98 g./mol | Molecular Formula: | C₉H₉BF₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08235087 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its boronic acid group facilitates coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for developing complex aromatic molecules. The presence of a trifluoroethylcarboxamide moiety adds polarity and metabolic stability, which is beneficial in drug design. Commonly employed in the synthesis of bioactive molecules and functional materials where fluorinated groups enhance lipophilicity and binding selectivity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $152.16 |
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| 0.100 | 10-20 days | $78.85 |
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(4-((2,2,2-Trifluoroethyl)carbamoyl)phenyl)boronic acid
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its boronic acid group facilitates coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for developing complex aromatic molecules. The presence of a trifluoroethylcarboxamide moiety adds polarity and metabolic stability, which is beneficial in drug design. Commonly employed in the synthesis of bioactive molecules and functional materials where fluorinated groups enhance lipophilicity and binding selectivity.
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