(R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-4-(tert-butoxycarbonyl)-5-oxopentanoic acid
98%
- Product Code: 231058
CAS:
111662-65-8
| Molecular Weight: | 525.590 g./mol | Molecular Formula: | C₂₉H₃₅NO₈ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00672341 | |
| Melting Point: | Boiling Point: | 695.3±55.0 °C(Predicted) | |
| Density: | 1.217±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily in peptide synthesis as a chiral building block, this compound serves as a protected amino acid derivative that enables the controlled assembly of complex peptides. Its structure includes orthogonal protecting groups—Fmoc and tert-butyl ester—that allow selective deprotection under mild conditions, making it ideal for solid-phase peptide synthesis. The presence of stereochemistry ensures the formation of peptides with defined three-dimensional architecture, which is critical for biological activity in pharmaceutical research. It is especially valuable in the preparation of enzyme inhibitors, bioactive peptides, and peptidomimetics where precise stereochemical configuration is required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft182,213.42 |
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| 0.250 | 10-20 days | Ft341,518.81 |
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| 1.000 | 10-20 days | Ft838,454.94 |
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(R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-4-(tert-butoxycarbonyl)-5-oxopentanoic acid
Used primarily in peptide synthesis as a chiral building block, this compound serves as a protected amino acid derivative that enables the controlled assembly of complex peptides. Its structure includes orthogonal protecting groups—Fmoc and tert-butyl ester—that allow selective deprotection under mild conditions, making it ideal for solid-phase peptide synthesis. The presence of stereochemistry ensures the formation of peptides with defined three-dimensional architecture, which is critical for biological activity in pharmaceutical research. It is especially valuable in the preparation of enzyme inhibitors, bioactive peptides, and peptidomimetics where precise stereochemical configuration is required.
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