2,4,6-Triisopropylphenylboronic acid
95%
- Product Code: 78542
CAS:
154549-38-9
| Molecular Weight: | 248.17 g./mol | Molecular Formula: | C₁₅H₂₅BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02683099 | |
| Melting Point: | 165ºC | Boiling Point: | 346.8ºC at 760mmHg |
| Density: | 0.97g/cm3 | Storage Condition: | 2-8°C |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and receptor antagonists. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the production of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to modify electronic properties. Additionally, it serves as a building block in the creation of functionalized polymers and coatings, enhancing their performance and stability. Its boronic acid group makes it valuable in sensing applications, particularly for detecting sugars and other diol-containing compounds.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 94.5 100% |
| Appearance | White to Faint Yellow to Yellow or Faint Brown to Brown Powder or Crystals |
| Proton NMR Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿550.00 |
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| 5.000 | 10-20 days | ฿1,980.00 |
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| 25.000 | 10-20 days | ฿7,500.00 |
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2,4,6-Triisopropylphenylboronic acid
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and receptor antagonists. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the production of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to modify electronic properties. Additionally, it serves as a building block in the creation of functionalized polymers and coatings, enhancing their performance and stability. Its boronic acid group makes it valuable in sensing applications, particularly for detecting sugars and other diol-containing compounds.
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