(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)oct-7-enoic acid
97%
- Product Code: 235102
CAS:
1251904-51-4
| Molecular Weight: | 379.45 g./mol | Molecular Formula: | C₂₃H₂₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03094929 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Widely used in peptide synthesis, this compound serves as a protected amino acid building block, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group provides temporary protection to the amino terminus, allowing selective coupling of amino acids in a controlled sequence. Its (S)-configuration ensures stereochemical consistency in the resulting peptides, making it valuable for producing biologically active peptides with high purity. The presence of the oct-7-enoic acid side chain introduces a reactive alkene handle, enabling further modification via thiol-ene chemistry or other alkene-based reactions for conjugation, labeling, or immobilization. This makes the compound especially useful in the development of peptide-based drugs, bioconjugates, and functional biomaterials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿7,410.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)oct-7-enoic acid
Widely used in peptide synthesis, this compound serves as a protected amino acid building block, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group provides temporary protection to the amino terminus, allowing selective coupling of amino acids in a controlled sequence. Its (S)-configuration ensures stereochemical consistency in the resulting peptides, making it valuable for producing biologically active peptides with high purity. The presence of the oct-7-enoic acid side chain introduces a reactive alkene handle, enabling further modification via thiol-ene chemistry or other alkene-based reactions for conjugation, labeling, or immobilization. This makes the compound especially useful in the development of peptide-based drugs, bioconjugates, and functional biomaterials.
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