4-Formylphenylboronic acid
>98%
- Product Code: 90707
Alias:
4-Formylphenylboronic acid; p-formylphenylboronic acid, p-formylphenylboronic acid
CAS:
87199-17-5
| Molecular Weight: | 149.94 g./mol | Molecular Formula: | C₇H₇BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00151823 | |
| Melting Point: | 237-242 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, it facilitates the formation of carbon-carbon bonds, essential in synthesizing complex organic molecules. It is also employed in the development of sensors for detecting sugars and other diol-containing compounds due to its ability to form reversible covalent bonds with 1,2- or 1,3-diols. Additionally, it serves as a building block in the preparation of pharmaceutical intermediates and materials for organic electronics. Its aldehyde group allows for further functionalization, making it versatile in organic synthesis and material science.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 97-100 |
| APPEARANCE | White to off-whtie to yellow powder |
| INFRARED SPECTRUM | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿320.00 |
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| 5.000 | 10-20 days | ฿660.00 |
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| 25.000 | 10-20 days | ฿1,960.00 |
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| 100.000 | 10-20 days | ฿6,220.00 |
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4-Formylphenylboronic acid
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, it facilitates the formation of carbon-carbon bonds, essential in synthesizing complex organic molecules. It is also employed in the development of sensors for detecting sugars and other diol-containing compounds due to its ability to form reversible covalent bonds with 1,2- or 1,3-diols. Additionally, it serves as a building block in the preparation of pharmaceutical intermediates and materials for organic electronics. Its aldehyde group allows for further functionalization, making it versatile in organic synthesis and material science.
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