(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpent-4-enoic acid
97%
- Product Code: 234997
CAS:
288617-71-0
| Molecular Weight: | 351.4 g./mol | Molecular Formula: | C₂₁H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02682444 | |
| Melting Point: | Boiling Point: | 564.2°C | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Widely used in peptide synthesis, this compound serves as a chiral building block for introducing allyl-containing amino acid residues with high stereocontrol. Its Fmoc protection allows for mild deprotection conditions compatible with solid-phase synthesis, making it ideal for constructing complex peptides and modified proteins. The terminal alkene in the side chain enables further functionalization via cross-metathesis or hydrofunctionalization reactions, facilitating the introduction of labels, tags, or cyclic structures through ring-closing metathesis. It is particularly valuable in the development of peptide-based drugs, macrocyclic compounds, and bioconjugates where precise stereochemistry and side-chain versatility are critical.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25mg | 10-20 days | ฿1,120.00 |
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| 100mg | 10-20 days | ฿3,720.00 |
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| 250mg | 10-20 days | ฿5,940.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpent-4-enoic acid
Widely used in peptide synthesis, this compound serves as a chiral building block for introducing allyl-containing amino acid residues with high stereocontrol. Its Fmoc protection allows for mild deprotection conditions compatible with solid-phase synthesis, making it ideal for constructing complex peptides and modified proteins. The terminal alkene in the side chain enables further functionalization via cross-metathesis or hydrofunctionalization reactions, facilitating the introduction of labels, tags, or cyclic structures through ring-closing metathesis. It is particularly valuable in the development of peptide-based drugs, macrocyclic compounds, and bioconjugates where precise stereochemistry and side-chain versatility are critical.
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