2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)propanoic acid
95%
- Product Code: 62330
CAS:
680579-19-5
| Molecular Weight: | 258.31 g./mol | Molecular Formula: | C₁₂H₂₂N₂O₄ |
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| EC Number: | MDL Number: | MFCD03410260 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of drug candidates, particularly those targeting neurological and cardiovascular diseases. The tert-butoxycarbonyl (Boc) protecting group in the compound is crucial for safeguarding the piperazine moiety during synthetic processes, allowing for selective reactions to occur. Additionally, it serves as an intermediate in the synthesis of peptides and other biologically active compounds, where the piperazine ring contributes to the desired pharmacological properties. Its application extends to research settings, where it is utilized in the study of biochemical pathways and the development of novel therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft23,756.91 |
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| 0.250 | 10-20 days | Ft39,271.62 |
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| 1.000 | 10-20 days | Ft87,270.27 |
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2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)propanoic acid
This chemical is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of drug candidates, particularly those targeting neurological and cardiovascular diseases. The tert-butoxycarbonyl (Boc) protecting group in the compound is crucial for safeguarding the piperazine moiety during synthetic processes, allowing for selective reactions to occur. Additionally, it serves as an intermediate in the synthesis of peptides and other biologically active compounds, where the piperazine ring contributes to the desired pharmacological properties. Its application extends to research settings, where it is utilized in the study of biochemical pathways and the development of novel therapeutic agents.
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