2,5-Dimethylphenylboronic acid
97%
- Product Code: 89581
Alias:
2,5-Dimethylphenylboronic acid
CAS:
85199-06-0
| Molecular Weight: | 149.98 g./mol | Molecular Formula: | C₈H₁₁BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01863525 | |
| Melting Point: | 186-191 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
2,5-Dimethylphenylboronic 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 acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its stability and reactivity make it a preferred choice in catalytic processes, enabling the creation of diverse chemical structures with high precision. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with specific biological targets.
Product Specification:
| Test | Specification |
|---|---|
| LOSS ON DRYING | 0-0.5 |
| Purity | 97-100 |
| APPEARANCE | Off-white powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $16.61 |
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| 5.000 | 10-20 days | $44.85 |
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| 25.000 | 10-20 days | $183.56 |
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| 100.000 | 10-20 days | $588.88 |
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2,5-Dimethylphenylboronic acid
2,5-Dimethylphenylboronic 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 acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its stability and reactivity make it a preferred choice in catalytic processes, enabling the creation of diverse chemical structures with high precision. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with specific biological targets.
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