(4-(4-methylpiperazin-1-yl)-2-(trifluoromethyl)phenyl)boronic acid
95%
- Product Code: 58209
CAS:
2225181-62-2
| Molecular Weight: | 288.0738496 g./mol | Molecular Formula: | C₁₂H₁₆BF₃N₂O₂ |
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| Density: | Storage Condition: | -20℃ |
Product Description:
This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of kinase inhibitors. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery. Additionally, it is employed in the preparation of targeted therapies for diseases such as cancer, where its structure contributes to the modulation of specific enzymatic pathways. Its trifluoromethyl group enhances metabolic stability and bioavailability, making it a crucial component in the design of potent and selective drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.010 | 10-20 days | £323.24 |
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| 0.025 | 10-20 days | £567.51 |
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(4-(4-methylpiperazin-1-yl)-2-(trifluoromethyl)phenyl)boronic acid
This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of kinase inhibitors. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery. Additionally, it is employed in the preparation of targeted therapies for diseases such as cancer, where its structure contributes to the modulation of specific enzymatic pathways. Its trifluoromethyl group enhances metabolic stability and bioavailability, making it a crucial component in the design of potent and selective drug candidates.
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