4-Methyl-3-(3-(4-methylpiperazin-1-yl)propoxy)phenylboronic acid
98%
- Product Code: 90674
CAS:
1704064-31-2
| Molecular Weight: | 292.19 g./mol | Molecular Formula: | C₁₅H₂₅BN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384332 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex drug molecules. It is particularly valuable in the development of kinase inhibitors, which are crucial for targeted cancer therapies. Additionally, its piperazine moiety enhances solubility and bioavailability, making it a preferred choice in drug design. The compound's unique structure also allows for modifications to optimize pharmacokinetic properties, aiding in the creation of more effective and selective therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | $774.41 |
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4-Methyl-3-(3-(4-methylpiperazin-1-yl)propoxy)phenylboronic acid
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex drug molecules. It is particularly valuable in the development of kinase inhibitors, which are crucial for targeted cancer therapies. Additionally, its piperazine moiety enhances solubility and bioavailability, making it a preferred choice in drug design. The compound's unique structure also allows for modifications to optimize pharmacokinetic properties, aiding in the creation of more effective and selective therapeutic agents.
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