(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methoxybutanoic acid
98%
- Product Code: 231171
CAS:
1272755-48-2
| Molecular Weight: | 355.38 g./mol | Molecular Formula: | C₂₀H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07366856 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed |
Product Description:
Used primarily in peptide synthesis as a chiral building block, this compound serves as a protected amino acid derivative featuring a methoxy group on the side chain. The Fmoc group enables orthogonal protection strategies in solid-phase peptide synthesis, allowing selective deprotection under mild basic conditions while maintaining stability during coupling steps. Its (R)-configuration is valuable for introducing stereochemically defined, non-natural amino acid motifs into peptides, which can influence conformation, bioavailability, and receptor selectivity. The methoxybutanoic acid side chain can act as a mimic for natural amino acid residues or serve as a functional handle for further modification, making it useful in the development of peptidomimetics, enzyme inhibitors, and pharmaceutical research intermediates.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €122.09 |
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| 0.250 | 10-20 days | €199.00 |
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| 1.000 | 10-20 days | €559.46 |
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| 5.000 | 10-20 days | €2,284.35 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methoxybutanoic acid
Used primarily in peptide synthesis as a chiral building block, this compound serves as a protected amino acid derivative featuring a methoxy group on the side chain. The Fmoc group enables orthogonal protection strategies in solid-phase peptide synthesis, allowing selective deprotection under mild basic conditions while maintaining stability during coupling steps. Its (R)-configuration is valuable for introducing stereochemically defined, non-natural amino acid motifs into peptides, which can influence conformation, bioavailability, and receptor selectivity. The methoxybutanoic acid side chain can act as a mimic for natural amino acid residues or serve as a functional handle for further modification, making it useful in the development of peptidomimetics, enzyme inhibitors, and pharmaceutical research intermediates.
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