(S)-2-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-oxo-4-(tritylamino)butanamido)acetic acid
98%
- Product Code: 236628
CAS:
1260093-07-9
| Molecular Weight: | 653.72 g./mol | Molecular Formula: | C₄₀H₃₅N₃O₆ |
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| EC Number: | MDL Number: | MFCD05663443 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry |
Product Description:
Used primarily in solid-phase peptide synthesis as a protected amino acid derivative, enabling stepwise assembly of peptides with high selectivity. The Fmoc group allows for mild base deprotection, while the trityl group protects side chains, preventing unwanted reactions. Its structure supports efficient coupling and deprotection cycles, making it valuable in synthesizing complex peptides for pharmaceutical research and development. Commonly applied in automated synthesizers for producing peptide-based drugs and biochemical probes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿3,210.00 |
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| 250mg | 10-20 days | ฿5,450.00 |
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| 1g | 10-20 days | ฿14,700.00 |
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| 5g | 10-20 days | ฿55,720.00 |
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(S)-2-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-oxo-4-(tritylamino)butanamido)acetic acid
Used primarily in solid-phase peptide synthesis as a protected amino acid derivative, enabling stepwise assembly of peptides with high selectivity. The Fmoc group allows for mild base deprotection, while the trityl group protects side chains, preventing unwanted reactions. Its structure supports efficient coupling and deprotection cycles, making it valuable in synthesizing complex peptides for pharmaceutical research and development. Commonly applied in automated synthesizers for producing peptide-based drugs and biochemical probes.
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| Stable in pH range | - |
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| INCI | - |
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