(4-Chloro-3-(4-ethylpiperazine-1-carbonyl)phenyl)boronic acid
98%
- Product Code: 89302
CAS:
1704074-11-2
| Molecular Weight: | 296.56 g./mol | Molecular Formula: | C₁₃H₁₈BClN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28384313 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of protease inhibitors and other therapeutic agents. 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 and material science. Additionally, its structure, featuring both a piperazine moiety and a boronic acid group, enhances its potential in targeting enzymes and receptors involved in disease pathways, making it a promising candidate for medicinal chemistry applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | $580.58 |
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(4-Chloro-3-(4-ethylpiperazine-1-carbonyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of protease inhibitors and other therapeutic agents. 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 and material science. Additionally, its structure, featuring both a piperazine moiety and a boronic acid group, enhances its potential in targeting enzymes and receptors involved in disease pathways, making it a promising candidate for medicinal chemistry applications.
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