(S)-2-((tert-Butoxycarbonyl)amino)-6-hydroxyhexanoic acid
95%
- Product Code: 51356
CAS:
77611-37-1
| Molecular Weight: | 247.29 g./mol | Molecular Formula: | C₁₁H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01862292 | |
| Melting Point: | 110-112°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used as an intermediate in the synthesis of complex organic compounds, particularly in the pharmaceutical industry. It plays a crucial role in the production of peptide-based drugs, where it serves as a building block for incorporating specific amino acid structures into larger molecules. Its hydroxyl and amino functional groups make it valuable for creating biologically active compounds, such as enzyme inhibitors or receptor modulators. Additionally, it is utilized in research and development for designing novel therapeutic agents, especially in the field of targeted drug delivery systems. Its stability and reactivity under controlled conditions make it a preferred choice for advanced organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,917.00 |
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| 0.250 | 10-20 days | ฿3,654.00 |
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| 1.000 | 10-20 days | ฿7,353.00 |
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| 5.000 | 10-20 days | ฿29,574.00 |
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(S)-2-((tert-Butoxycarbonyl)amino)-6-hydroxyhexanoic acid
This chemical is primarily used as an intermediate in the synthesis of complex organic compounds, particularly in the pharmaceutical industry. It plays a crucial role in the production of peptide-based drugs, where it serves as a building block for incorporating specific amino acid structures into larger molecules. Its hydroxyl and amino functional groups make it valuable for creating biologically active compounds, such as enzyme inhibitors or receptor modulators. Additionally, it is utilized in research and development for designing novel therapeutic agents, especially in the field of targeted drug delivery systems. Its stability and reactivity under controlled conditions make it a preferred choice for advanced organic synthesis.
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