(S)-3-((tert-Butoxycarbonyl)amino)-4-(naphthalen-1-yl)butanoic acid
98%
- Product Code: 60703
CAS:
219297-09-3
| Molecular Weight: | 329.39 g./mol | Molecular Formula: | C₁₉H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01076282 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the synthesis of peptides and peptidomimetics, particularly in the development of biologically active compounds. It serves as a key intermediate in the production of pharmaceutical agents, especially those targeting specific enzymes or receptors. Its structure, featuring a naphthalene group, makes it valuable in creating molecules with enhanced binding affinity and selectivity. Additionally, it is utilized in research for designing inhibitors or modulators of protein-protein interactions, contributing to drug discovery efforts in areas such as cancer, inflammation, and infectious diseases. Its tert-butoxycarbonyl (Boc) protecting group allows for controlled deprotection during synthetic processes, ensuring precise construction of complex molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,375.00 |
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(S)-3-((tert-Butoxycarbonyl)amino)-4-(naphthalen-1-yl)butanoic acid
This chemical is primarily used in the synthesis of peptides and peptidomimetics, particularly in the development of biologically active compounds. It serves as a key intermediate in the production of pharmaceutical agents, especially those targeting specific enzymes or receptors. Its structure, featuring a naphthalene group, makes it valuable in creating molecules with enhanced binding affinity and selectivity. Additionally, it is utilized in research for designing inhibitors or modulators of protein-protein interactions, contributing to drug discovery efforts in areas such as cancer, inflammation, and infectious diseases. Its tert-butoxycarbonyl (Boc) protecting group allows for controlled deprotection during synthetic processes, ensuring precise construction of complex molecules.
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