(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-methoxy-2-methylphenyl)propanoic acid
95%
- Product Code: 236849
CAS:
2276402-03-8
| Molecular Weight: | 431.48 g./mol | Molecular Formula: | C₂₆H₂₅NO₅ |
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| Density: | Storage Condition: | 2-8°C, light-proof, inert gas |
Product Description:
Used primarily in peptide synthesis as a protected amino acid derivative, enabling the construction of complex peptides with high stereochemical control. The Fmoc group allows for mild base-labile protection, making it ideal for solid-phase peptide synthesis (SPPS). Its aromatic and methoxy substituents enhance solubility and stability during coupling steps. Commonly employed in the preparation of pharmaceutical intermediates, especially in the development of bioactive peptides and peptidomimetics. The compound’s chiral center ensures enantioselective synthesis, critical for achieving biologically active peptide structures.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | ฿6,280.00 |
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| 100mg | 10-20 days | ฿8,180.00 |
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| 250mg | 10-20 days | ฿13,630.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-methoxy-2-methylphenyl)propanoic acid
Used primarily in peptide synthesis as a protected amino acid derivative, enabling the construction of complex peptides with high stereochemical control. The Fmoc group allows for mild base-labile protection, making it ideal for solid-phase peptide synthesis (SPPS). Its aromatic and methoxy substituents enhance solubility and stability during coupling steps. Commonly employed in the preparation of pharmaceutical intermediates, especially in the development of bioactive peptides and peptidomimetics. The compound’s chiral center ensures enantioselective synthesis, critical for achieving biologically active peptide structures.
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