3,5-Dimethoxyphenylboronic acid
95%
- Product Code: 89943
Alias:
3,5-Dimethoxyphenylboronic acid
CAS:
192182-54-0
| Molecular Weight: | 181.98 g./mol | Molecular Formula: | C₈H₁₁BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03095127 | |
| Melting Point: | 205-207°C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create complex biaryl compounds. These compounds are essential in pharmaceuticals, agrochemicals, and materials science. It also serves as a building block for developing fluorescent probes and sensors, aiding in biochemical research and diagnostics. Its boronic acid group enables selective binding to diols, making it useful in carbohydrate recognition and glycobiology studies. Additionally, it is employed in the preparation of organic electronic materials, contributing to advancements in OLEDs and other optoelectronic devices.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 94.5-100 |
| PURITYTITRATION BY NAOH | 94.5-102.5 |
| APPEARANCE | WHITE TO TAN OR YELLOW CRYSTALS, POWDER OR SOLID |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿400.00 |
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| 5.000 | 10-20 days | ฿1,700.00 |
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| 25.000 | 10-20 days | ฿7,850.00 |
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3,5-Dimethoxyphenylboronic acid
Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create complex biaryl compounds. These compounds are essential in pharmaceuticals, agrochemicals, and materials science. It also serves as a building block for developing fluorescent probes and sensors, aiding in biochemical research and diagnostics. Its boronic acid group enables selective binding to diols, making it useful in carbohydrate recognition and glycobiology studies. Additionally, it is employed in the preparation of organic electronic materials, contributing to advancements in OLEDs and other optoelectronic devices.
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