(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((tert-butoxycarbonyl)amino)butanoic acid
97%
- Product Code: 236578
CAS:
1310680-44-4
| Molecular Weight: | 440.49 g./mol | Molecular Formula: | C₂₄H₂₈N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08457841 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used in peptide synthesis as a protected amino acid building block, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group allows for orthogonal protection of the alpha-amino group, enabling stepwise assembly of peptides with mild base-labile deprotection. The tert-butoxycarbonyl (Boc) group protects the side-chain amine, making it suitable for incorporating asparagine or aspartic acid derivatives selectively. Its stereochemistry ensures chiral purity in the resulting peptide chain. Commonly employed in the preparation of complex peptides and proteins for pharmaceutical and biochemical research.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,920.00 |
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| 0.250 | 10-20 days | ฿10,340.00 |
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| 1.000 | 10-20 days | ฿25,820.00 |
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((tert-butoxycarbonyl)amino)butanoic acid
Used in peptide synthesis as a protected amino acid building block, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group allows for orthogonal protection of the alpha-amino group, enabling stepwise assembly of peptides with mild base-labile deprotection. The tert-butoxycarbonyl (Boc) group protects the side-chain amine, making it suitable for incorporating asparagine or aspartic acid derivatives selectively. Its stereochemistry ensures chiral purity in the resulting peptide chain. Commonly employed in the preparation of complex peptides and proteins for pharmaceutical and biochemical research.
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