(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(allyloxy)phenyl)propanoic acid
≥98%
- Product Code: 38154
CAS:
1175973-95-1
Molecular Weight: | 443.49 g./mol | Molecular Formula: | C₂₇H₂₅NO₅ |
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EC Number: | MDL Number: | MFCD08061623 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amine functionality, enabling selective deprotection during solid-phase peptide synthesis. The allyloxy group on the phenyl ring can be utilized for further functionalization or as a protective group that can be removed under mild conditions. Its application is significant in the development of complex peptides and proteins, particularly in pharmaceutical research and bioconjugation studies. The compound’s structure allows for precise control over peptide assembly, making it valuable in the synthesis of bioactive peptides and peptidomimetics.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,530.00 |
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0.250 | 10-20 days | ฿2,700.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(allyloxy)phenyl)propanoic acid
This compound is primarily used in peptide synthesis as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amine functionality, enabling selective deprotection during solid-phase peptide synthesis. The allyloxy group on the phenyl ring can be utilized for further functionalization or as a protective group that can be removed under mild conditions. Its application is significant in the development of complex peptides and proteins, particularly in pharmaceutical research and bioconjugation studies. The compound’s structure allows for precise control over peptide assembly, making it valuable in the synthesis of bioactive peptides and peptidomimetics.
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