(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-((allyloxy)carbonyl)phenyl)propanoic acid
95%
- Product Code: 233263
CAS:
2196198-73-7
| Molecular Weight: | 471.5 g./mol | Molecular Formula: | C₂₈H₂₅NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 703.1±60.0 °C(Predicted) | |
| Density: | 1.276±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for incorporating phenylalanine analogs into peptide chains. The Fmoc group provides temporary protection for the amine functionality, allowing for stepwise assembly of peptides under mild basic conditions. The allyl ester protection on the aromatic ring offers orthogonal stability, enabling selective deprotection in the presence of other functional groups. This feature is particularly valuable in solid-phase peptide synthesis where precise control over reactivity is required. Additionally, the allyl group can be cleanly removed using palladium catalysts, minimizing side reactions. Its structure supports the synthesis of complex peptides and modified proteins used in pharmaceutical research and development.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $308.78 |
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| 0.250 | 10-20 days | $523.79 |
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| 1.000 | 10-20 days | $1,413.35 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-((allyloxy)carbonyl)phenyl)propanoic acid
Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for incorporating phenylalanine analogs into peptide chains. The Fmoc group provides temporary protection for the amine functionality, allowing for stepwise assembly of peptides under mild basic conditions. The allyl ester protection on the aromatic ring offers orthogonal stability, enabling selective deprotection in the presence of other functional groups. This feature is particularly valuable in solid-phase peptide synthesis where precise control over reactivity is required. Additionally, the allyl group can be cleanly removed using palladium catalysts, minimizing side reactions. Its structure supports the synthesis of complex peptides and modified proteins used in pharmaceutical research and development.
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