3-(Ethylcarbamoyl)benzeneboronic acid
97%
- Product Code: 185918
CAS:
850567-21-4
| Molecular Weight: | 193.01 g./mol | Molecular Formula: | C₉H₁₂BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04115689 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical intermediates. Its boronic acid group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in drug discovery and development. The ethylcarbamoyl moiety adds polarity and hydrogen-bonding capability, which can influence the biological activity and solubility of resulting compounds. Commonly employed in the preparation of bioactive molecules, including potential therapeutic agents targeting enzymes and receptors.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿4,580.00 |
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| 1.000 G | 10-20 days | ฿8,770.00 |
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| 5.000 G | 10-20 days | ฿26,310.00 |
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| 25.000 G | 10-20 days | ฿96,100.00 |
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3-(Ethylcarbamoyl)benzeneboronic acid
Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical intermediates. Its boronic acid group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in drug discovery and development. The ethylcarbamoyl moiety adds polarity and hydrogen-bonding capability, which can influence the biological activity and solubility of resulting compounds. Commonly employed in the preparation of bioactive molecules, including potential therapeutic agents targeting enzymes and receptors.
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