(2-Methoxy-5-(methoxycarbonyl)phenyl)boronic acid
95%, containing varying amounts of acid anhydrides
- Product Code: 61873
CAS:
221006-63-9
| Molecular Weight: | 209.99 g./mol | Molecular Formula: | C₉H₁₁BO₅ |
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| EC Number: | MDL Number: | MFCD09800877 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create carbon-carbon bonds, enabling the synthesis of bioactive compounds and drug candidates. Its boronic acid group is essential for coupling with aryl halides, making it valuable in constructing biaryl structures. Additionally, it finds application in material science for developing organic electronic materials and polymers. Its methoxy and methoxycarbonyl substituents enhance its reactivity and compatibility in various catalytic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $133.06 |
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| 0.250 | 10-20 days | $225.75 |
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| 1.000 | 10-20 days | $584.56 |
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| 5.000 | 10-20 days | $2,805.82 |
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(2-Methoxy-5-(methoxycarbonyl)phenyl)boronic acid
Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create carbon-carbon bonds, enabling the synthesis of bioactive compounds and drug candidates. Its boronic acid group is essential for coupling with aryl halides, making it valuable in constructing biaryl structures. Additionally, it finds application in material science for developing organic electronic materials and polymers. Its methoxy and methoxycarbonyl substituents enhance its reactivity and compatibility in various catalytic processes.
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