(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-5-((tert-butoxycarbonyl)amino)pentanoicacid
97%
- Product Code: 237766
CAS:
1793105-28-8
| Molecular Weight: | 468.54 g./mol | Molecular Formula: | C₂₆H₃₂N₂O₆ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | Room temperature |
Product Description:
Widely used in peptide synthesis, this compound serves as a protected amino acid building block, particularly for incorporating glutamine or glutamate derivatives with stereochemical control. The Fmoc group allows for mild base-labile protection of the alpha-amine, enabling stepwise assembly of peptides using solid-phase techniques. The tert-butoxycarbonyl (Boc) group on the side chain protects an additional amine or carboxylic acid functionality, depending on the synthetic strategy, and is stable under basic conditions but removable with mild acid. Its stereochemistry ensures chiral integrity during coupling, making it valuable for synthesizing biologically active peptides where configuration affects function. Commonly employed in pharmaceutical research, it aids in the production of peptide-based drugs, diagnostics, and biochemical probes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿4,200.00 |
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| 250mg | 10-20 days | ฿7,030.00 |
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| 5g | 10-20 days | ฿61,560.00 |
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| 1g | 10-20 days | ฿19,500.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-5-((tert-butoxycarbonyl)amino)pentanoicacid
Widely used in peptide synthesis, this compound serves as a protected amino acid building block, particularly for incorporating glutamine or glutamate derivatives with stereochemical control. The Fmoc group allows for mild base-labile protection of the alpha-amine, enabling stepwise assembly of peptides using solid-phase techniques. The tert-butoxycarbonyl (Boc) group on the side chain protects an additional amine or carboxylic acid functionality, depending on the synthetic strategy, and is stable under basic conditions but removable with mild acid. Its stereochemistry ensures chiral integrity during coupling, making it valuable for synthesizing biologically active peptides where configuration affects function. Commonly employed in pharmaceutical research, it aids in the production of peptide-based drugs, diagnostics, and biochemical probes.
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