4-(3′-(Trifluoromethyl)phenoxymethyl)phenylboronic acid
≥98%
- Product Code: 66337
CAS:
849062-03-9
| Molecular Weight: | 296.05 g./mol | Molecular Formula: | C₁₄H₁₂BF₃O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07369740 | |
| Melting Point: | Boiling Point: | 416.7ºC | |
| Density: | 1.33g/cm3 | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the creation of complex organic molecules. Its trifluoromethyl and phenoxymethyl groups enhance its reactivity and selectivity, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for designing advanced polymers and functional materials. Its boronic acid moiety allows for efficient conjugation with various substrates, expanding its application in bioconjugation and sensor development.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | white solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿4,760.00 |
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4-(3′-(Trifluoromethyl)phenoxymethyl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the creation of complex organic molecules. Its trifluoromethyl and phenoxymethyl groups enhance its reactivity and selectivity, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for designing advanced polymers and functional materials. Its boronic acid moiety allows for efficient conjugation with various substrates, expanding its application in bioconjugation and sensor development.
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