5-(N-Methylpiperazin-1-yl)furan-2-boronic acid
95%
- Product Code: 48287
CAS:
2225170-17-0
| Molecular Weight: | 210.038 g./mol | Molecular Formula: | C₉H₁₅BN₂O₃ |
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| Density: | Storage Condition: | -20℃ |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and drug discovery, particularly in the synthesis of biologically active compounds. It serves as a key intermediate in the development of pharmaceutical agents, especially those targeting specific enzymes or receptors. The boronic acid group in its structure makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for creating carbon-carbon bonds in complex organic molecules. This property is essential for constructing diverse molecular frameworks in drug design. Additionally, its piperazine moiety contributes to enhancing the pharmacokinetic properties of potential drug candidates, such as solubility and bioavailability. Researchers often employ it in the preparation of compounds for studying disease mechanisms or screening for therapeutic activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.005 | 10-20 days | $239.23 |
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| 0.025 | 10-20 days | $934.11 |
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5-(N-Methylpiperazin-1-yl)furan-2-boronic acid
This chemical is primarily utilized in the field of medicinal chemistry and drug discovery, particularly in the synthesis of biologically active compounds. It serves as a key intermediate in the development of pharmaceutical agents, especially those targeting specific enzymes or receptors. The boronic acid group in its structure makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for creating carbon-carbon bonds in complex organic molecules. This property is essential for constructing diverse molecular frameworks in drug design. Additionally, its piperazine moiety contributes to enhancing the pharmacokinetic properties of potential drug candidates, such as solubility and bioavailability. Researchers often employ it in the preparation of compounds for studying disease mechanisms or screening for therapeutic activity.
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