(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-6-((tert-butoxycarbonyl)amino)hexanoic acid
95%
- Product Code: 231266
CAS:
1793105-27-7
| Molecular Weight: | 482.57 g./mol | Molecular Formula: | C₂₇H₃₄N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08702737 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Widely used in peptide synthesis, this compound serves as a protected amino acid building block, particularly for incorporating lysine derivatives with orthogonal protection. The Fmoc group allows for base-labile protection of the alpha-amine, enabling solid-phase peptide synthesis under mild conditions, while the tert-butoxycarbonyl (Boc) group protects the side-chain amine of the lysine moiety. This dual protection scheme permits selective deprotection and stepwise assembly of complex peptides. Its structure supports efficient coupling and minimal racemization, making it valuable in the preparation of pharmaceutical peptides, biochemical probes, and research reagents. Commonly employed in automated synthesizers, it facilitates the production of high-purity peptides for drug development and molecular biology studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,240.00 |
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| 250mg | 10-20 days | ฿3,040.00 |
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| 1g | 10-20 days | ฿6,160.00 |
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| 5g | 10-20 days | ฿26,790.00 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-6-((tert-butoxycarbonyl)amino)hexanoic acid
Widely used in peptide synthesis, this compound serves as a protected amino acid building block, particularly for incorporating lysine derivatives with orthogonal protection. The Fmoc group allows for base-labile protection of the alpha-amine, enabling solid-phase peptide synthesis under mild conditions, while the tert-butoxycarbonyl (Boc) group protects the side-chain amine of the lysine moiety. This dual protection scheme permits selective deprotection and stepwise assembly of complex peptides. Its structure supports efficient coupling and minimal racemization, making it valuable in the preparation of pharmaceutical peptides, biochemical probes, and research reagents. Commonly employed in automated synthesizers, it facilitates the production of high-purity peptides for drug development and molecular biology studies.
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