(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((2,2,10,10-tetramethyl-4,8-dioxo-3,9-dioxa-5,7-diazaundecan-6-ylidene)amino)butanoic acid
97%
- Product Code: 233524
CAS:
206183-06-4
| Molecular Weight: | 582.64 g./mol | Molecular Formula: | C₃₀H₃₈N₄O₈ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01632267 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.26±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, away from light, dry |
Product Description:
Used primarily in peptide synthesis as a protected amino acid derivative, this compound serves as a chiral building block for the preparation of complex peptides and proteins. Its structure incorporates a fluorenylmethyloxycarbonyl (Fmoc) group, which acts as a temporary protecting group for the alpha-amino function, allowing for stepwise assembly in solid-phase peptide synthesis. The presence of a specialized diamino linker with ketone and ether functionalities enables selective conjugation or cyclization strategies, making it valuable in the development of peptide-based drugs, macrocyclic peptides, and bioconjugates. Its stereochemistry supports the synthesis of enantiomerically pure peptides, important in pharmaceutical research where biological activity is highly stereospecific.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $223.05 |
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| 1.000 | 10-20 days | $1,022.21 |
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| 0.250 | 10-20 days | $378.55 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((2,2,10,10-tetramethyl-4,8-dioxo-3,9-dioxa-5,7-diazaundecan-6-ylidene)amino)butanoic acid
Used primarily in peptide synthesis as a protected amino acid derivative, this compound serves as a chiral building block for the preparation of complex peptides and proteins. Its structure incorporates a fluorenylmethyloxycarbonyl (Fmoc) group, which acts as a temporary protecting group for the alpha-amino function, allowing for stepwise assembly in solid-phase peptide synthesis. The presence of a specialized diamino linker with ketone and ether functionalities enables selective conjugation or cyclization strategies, making it valuable in the development of peptide-based drugs, macrocyclic peptides, and bioconjugates. Its stereochemistry supports the synthesis of enantiomerically pure peptides, important in pharmaceutical research where biological activity is highly stereospecific.
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