(S)-2-(((Benzyloxy)carbonyl)amino)-3-(naphthalen-1-yl)propanoic acid
95%
- Product Code: 57134
CAS:
65365-15-3
| Molecular Weight: | 349.38 g./mol | Molecular Formula: | C₂₁H₁₉NO₄ |
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| EC Number: | MDL Number: | MFCD00238419 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. Its structure, featuring a benzyloxycarbonyl (Cbz) protecting group, makes it valuable for constructing peptides with specific sequences, particularly those requiring the incorporation of naphthalene-based side chains. The Cbz group can be selectively removed under mild conditions, allowing for further functionalization or elongation of the peptide chain. Additionally, it finds applications in medicinal chemistry research, where it is used to develop peptide-based drugs or probes targeting biological systems. Its unique naphthalene moiety can contribute to enhanced binding affinity or fluorescence properties, making it useful in biochemical studies and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿8,730.00 |
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| 1.000 | 10-20 days | ฿21,753.00 |
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(S)-2-(((Benzyloxy)carbonyl)amino)-3-(naphthalen-1-yl)propanoic acid
This chemical is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. Its structure, featuring a benzyloxycarbonyl (Cbz) protecting group, makes it valuable for constructing peptides with specific sequences, particularly those requiring the incorporation of naphthalene-based side chains. The Cbz group can be selectively removed under mild conditions, allowing for further functionalization or elongation of the peptide chain. Additionally, it finds applications in medicinal chemistry research, where it is used to develop peptide-based drugs or probes targeting biological systems. Its unique naphthalene moiety can contribute to enhanced binding affinity or fluorescence properties, making it useful in biochemical studies and drug discovery.
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