4-Isobutylphenylboronic Acid
≥98%
- Product Code: 90568
CAS:
153624-38-5
| Molecular Weight: | 178.04 g./mol | Molecular Formula: | C₁₀H₁₅BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 117-120°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
4-Isobutylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including drug candidates and biologically active compounds. Its boronic acid group enables efficient and selective coupling with aryl halides, facilitating the creation of diverse chemical structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with diols and other functional groups, making it useful in analytical and industrial applications.
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 | ฿3,100.00 |
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4-Isobutylphenylboronic Acid
4-Isobutylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including drug candidates and biologically active compounds. Its boronic acid group enables efficient and selective coupling with aryl halides, facilitating the creation of diverse chemical structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with diols and other functional groups, making it useful in analytical and industrial applications.
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