Benzyl N-Boc-4-isopropyl-4-piperidinecarboxylate
≥97%
- Product Code: 76497
CAS:
1226776-80-2
| Molecular Weight: | 361.48 g./mol | Molecular Formula: | C₂₁H₃₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16495869 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of complex organic molecules. It serves as a key building block in the preparation of various biologically active compounds, including potential drug candidates. Its structure, featuring both Boc-protected amine and ester functional groups, makes it valuable in peptide synthesis and medicinal chemistry. The compound is often employed in research settings to explore new therapeutic agents, especially those targeting neurological disorders or other conditions requiring modulation of specific biological pathways. Its stability and reactivity under controlled conditions make it a preferred choice for multi-step synthetic processes in organic chemistry laboratories.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿7,542.00 |
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| 1.000 | 10-20 days | ฿16,254.00 |
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Benzyl N-Boc-4-isopropyl-4-piperidinecarboxylate
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of complex organic molecules. It serves as a key building block in the preparation of various biologically active compounds, including potential drug candidates. Its structure, featuring both Boc-protected amine and ester functional groups, makes it valuable in peptide synthesis and medicinal chemistry. The compound is often employed in research settings to explore new therapeutic agents, especially those targeting neurological disorders or other conditions requiring modulation of specific biological pathways. Its stability and reactivity under controlled conditions make it a preferred choice for multi-step synthetic processes in organic chemistry laboratories.
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