(4-Methylpiperazin-1-yl)(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanone
98%
- Product Code: 203029
CAS:
883738-38-3
| Molecular Weight: | 330.23 g./mol | Molecular Formula: | C₁₈H₂₇BN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05864308 | |
| Melting Point: | 86-89 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of biaryl and aryl-heteroaryl structures commonly found in pharmaceuticals and agrochemicals. The presence of the boronate ester group allows for efficient palladium-catalyzed coupling with aryl halides, making it valuable in the synthesis of complex organic molecules, particularly in drug discovery and development. Its piperazine-based scaffold contributes to improved solubility and binding properties in bioactive compounds, enhancing its utility in medicinal chemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿3,880.00 |
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| 5g | 10-20 days | ฿15,520.00 |
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(4-Methylpiperazin-1-yl)(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanone
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of biaryl and aryl-heteroaryl structures commonly found in pharmaceuticals and agrochemicals. The presence of the boronate ester group allows for efficient palladium-catalyzed coupling with aryl halides, making it valuable in the synthesis of complex organic molecules, particularly in drug discovery and development. Its piperazine-based scaffold contributes to improved solubility and binding properties in bioactive compounds, enhancing its utility in medicinal chemistry.
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