4-(benzyloxy)-3-fluorophenylboronic acid
98%
- Product Code: 90735
Alias:
4-Benzyloxy-3-fluorophenylboronic acid
CAS:
133057-83-7
| Molecular Weight: | 246.04 g./mol | Molecular Formula: | C₁₃H₁₂BFO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00994627 | |
| Melting Point: | 116 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its application is significant in pharmaceutical research, where it aids in the development of drug candidates by facilitating the synthesis of biologically active compounds. Additionally, it is used in material science for designing advanced polymers and functional materials. Its boronic acid group allows for selective binding to diols, making it useful in sensor development for detecting sugars and other analytes.
Product Specification:
| Test | Specification |
|---|---|
| PURITYLC | 98-100 |
| APPEARANCE | White to off-white powder |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿380.00 |
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| 1.000 | 10-20 days | ฿850.00 |
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| 5.000 | 10-20 days | ฿2,580.00 |
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4-(benzyloxy)-3-fluorophenylboronic acid
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its application is significant in pharmaceutical research, where it aids in the development of drug candidates by facilitating the synthesis of biologically active compounds. Additionally, it is used in material science for designing advanced polymers and functional materials. Its boronic acid group allows for selective binding to diols, making it useful in sensor development for detecting sugars and other analytes.
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