(3-(3-(Ethoxycarbonyl)piperidine-1-carbonyl)phenyl)boronic acid
96%
- Product Code: 185820
CAS:
1218790-81-8
| Molecular Weight: | 305.13 g./mol | Molecular Formula: | C₁₅H₂₀BNO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12756423 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, inert gas |
Product Description:
Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical development. Its boronic acid functionality allows it to react with aryl halides under palladium catalysis, making it valuable in constructing complex aromatic systems found in bioactive molecules. Commonly employed in the synthesis of drug candidates targeting central nervous system disorders and inflammatory diseases due to its structural compatibility with medicinal chemistry frameworks. The ethoxycarbonyl group enhances solubility and provides a handle for further functionalization, improving versatility in multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿2,480.00 |
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| 1.000 G | 10-20 days | ฿6,590.00 |
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| 5.000 G | 10-20 days | ฿22,820.00 |
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| 25.000 G | 10-20 days | ฿79,890.00 |
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(3-(3-(Ethoxycarbonyl)piperidine-1-carbonyl)phenyl)boronic acid
Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical development. Its boronic acid functionality allows it to react with aryl halides under palladium catalysis, making it valuable in constructing complex aromatic systems found in bioactive molecules. Commonly employed in the synthesis of drug candidates targeting central nervous system disorders and inflammatory diseases due to its structural compatibility with medicinal chemistry frameworks. The ethoxycarbonyl group enhances solubility and provides a handle for further functionalization, improving versatility in multi-step synthetic routes.
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