(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(thiazol-4-yl)propanoic acid
96%
- Product Code: 104192
CAS:
205528-33-2
| Molecular Weight: | 394.44 g./mol | Molecular Formula: | C₂₁H₁₈N₂O₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00672569 | |
| Melting Point: | Boiling Point: | 647.5°C at 760 mmHg | |
| 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. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective moiety for the amino group, ensuring selective reactions during the peptide chain assembly. Its structure, featuring a thiazol-4-yl group, makes it particularly useful in the synthesis of peptides with specific biological activities or for incorporating heterocyclic motifs into peptide sequences. It is commonly employed in solid-phase peptide synthesis (SPPS) methodologies, enabling the production of complex peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and compatibility with standard peptide coupling reagents make it a valuable tool in the preparation of peptide-based therapeutics and probes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,924.00 |
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| 1.000 | 10-20 days | ฿9,828.00 |
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| 5.000 | 10-20 days | ฿37,890.00 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(thiazol-4-yl)propanoic acid
This chemical is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective moiety for the amino group, ensuring selective reactions during the peptide chain assembly. Its structure, featuring a thiazol-4-yl group, makes it particularly useful in the synthesis of peptides with specific biological activities or for incorporating heterocyclic motifs into peptide sequences. It is commonly employed in solid-phase peptide synthesis (SPPS) methodologies, enabling the production of complex peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and compatibility with standard peptide coupling reagents make it a valuable tool in the preparation of peptide-based therapeutics and probes.
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