3-(4-(BOC-Piperazine-1-carbonyl)phenylboronic acid
98%
- Product Code: 65478
CAS:
1218790-82-9
| Molecular Weight: | 334.18 g./mol | Molecular Formula: | C₁₆H₂₃BN₂O₅ |
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| EC Number: | MDL Number: | MFCD12546575 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis and medicinal chemistry as a versatile building block. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The BOC-protected piperazine moiety enhances its utility in peptide and drug development, where it serves as a protected intermediate for introducing piperazine derivatives into target molecules. Additionally, its structure is suitable for designing protease inhibitors and other biologically active compounds, particularly in the development of drugs targeting neurological disorders and cancer. Its stability and reactivity make it a preferred choice in complex multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿20,740.00 |
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3-(4-(BOC-Piperazine-1-carbonyl)phenylboronic acid
This chemical is primarily used in organic synthesis and medicinal chemistry as a versatile building block. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The BOC-protected piperazine moiety enhances its utility in peptide and drug development, where it serves as a protected intermediate for introducing piperazine derivatives into target molecules. Additionally, its structure is suitable for designing protease inhibitors and other biologically active compounds, particularly in the development of drugs targeting neurological disorders and cancer. Its stability and reactivity make it a preferred choice in complex multi-step synthetic processes.
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