(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(4-(tert-butoxy)phenyl)butanoic acid
95%
- Product Code: 104350
CAS:
204384-69-0
| Molecular Weight: | 473.56 g./mol | Molecular Formula: | C₂₉H₃₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01321420 | |
| 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. The fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino functionality, enabling selective deprotection during solid-phase peptide synthesis. The tert-butoxy group on the phenyl ring provides additional protection for the side chain, ensuring stability during the synthesis process. Its application is crucial in the production of complex peptides, particularly in pharmaceutical research and development, where precise control over peptide sequences is required. The compound’s structure allows for efficient incorporation into peptide chains while maintaining the integrity of sensitive functional groups.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $461.56 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(4-(tert-butoxy)phenyl)butanoic 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 temporary protecting group for the amino functionality, enabling selective deprotection during solid-phase peptide synthesis. The tert-butoxy group on the phenyl ring provides additional protection for the side chain, ensuring stability during the synthesis process. Its application is crucial in the production of complex peptides, particularly in pharmaceutical research and development, where precise control over peptide sequences is required. The compound’s structure allows for efficient incorporation into peptide chains while maintaining the integrity of sensitive functional groups.
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