(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-7-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl)amino)heptanoic acid
97%
- Product Code: 233221
CAS:
2703745-40-6
| Molecular Weight: | 588.73 g./mol | Molecular Formula: | C₃₅H₄₄N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD34186940 | |
| Melting Point: | Boiling Point: | 775.6±60.0 °C(Predicted) | |
| Density: | 1.172±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, away from light, dry |
Product Description:
Used in peptide synthesis as a protected amino acid derivative, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group provides temporary protection for the amine functionality, allowing stepwise assembly of peptides with high selectivity. The compound’s structure supports incorporation into complex peptide sequences where sterically hindered or modified amino acids are required. Its design facilitates coupling reactions while minimizing side reactions, making it valuable in the production of therapeutic peptides and biochemical research tools. The 4,4-dimethyl-2,6-dioxocyclohexylidene moiety can act as a protecting group for side chains, especially in lysine analogs, enabling orthogonal deprotection strategies during synthesis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | ฿10,370.00 |
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| 100mg | 10-20 days | ฿17,630.00 |
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-7-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl)amino)heptanoic acid
Used in peptide synthesis as a protected amino acid derivative, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group provides temporary protection for the amine functionality, allowing stepwise assembly of peptides with high selectivity. The compound’s structure supports incorporation into complex peptide sequences where sterically hindered or modified amino acids are required. Its design facilitates coupling reactions while minimizing side reactions, making it valuable in the production of therapeutic peptides and biochemical research tools. The 4,4-dimethyl-2,6-dioxocyclohexylidene moiety can act as a protecting group for side chains, especially in lysine analogs, enabling orthogonal deprotection strategies during synthesis.
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