(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-phenylpent-4-enoic acid
98%
- Product Code: 104201
CAS:
215190-23-1
| Molecular Weight: | 413.47 g./mol | Molecular Formula: | C₂₆H₂₃NO₄ |
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| EC Number: | MDL Number: | MFCD01311775 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality, ensuring selective reactions during peptide chain assembly. Its structure, including the phenylpent-4-enoic acid moiety, makes it suitable for introducing specific side-chain functionalities into peptides. It is commonly employed in research and development of pharmaceuticals, bioactive peptides, and protein studies, where precise control over peptide sequence and structure is crucial.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | £61.07 |
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| 1.000 | 10-20 days | £155.72 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-phenylpent-4-enoic acid
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality, ensuring selective reactions during peptide chain assembly. Its structure, including the phenylpent-4-enoic acid moiety, makes it suitable for introducing specific side-chain functionalities into peptides. It is commonly employed in research and development of pharmaceuticals, bioactive peptides, and protein studies, where precise control over peptide sequence and structure is crucial.
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