4-Iodophenylboronic acid
98%
- Product Code: 90711
Alias:
p-Iodophenylboronic acid
CAS:
5122-99-6
| Molecular Weight: | 247.83 g./mol | Molecular Formula: | C₆H₆BIO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01319014 | |
| Melting Point: | 326-330 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating biaryl structures. These reactions are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and sugars, making it valuable in biochemical and diagnostic applications. Its iodine substituent also allows for further functionalization, enhancing its versatility in synthetic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98 100% |
| MP | 326 330? |
| APPEARANCE | White to off white powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿400.00 |
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| 5.000 | 10-20 days | ฿1,760.00 |
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| 25.000 | 10-20 days | ฿8,230.00 |
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4-Iodophenylboronic acid
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating biaryl structures. These reactions are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and sugars, making it valuable in biochemical and diagnostic applications. Its iodine substituent also allows for further functionalization, enhancing its versatility in synthetic chemistry.
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