(R)-N-Fmoc-2-(4'-pentenyl)glycine
>97%
- Product Code: 230205
CAS:
1093645-21-6
| Molecular Weight: | 365.42 g./mol | Molecular Formula: | C₂₂H₂₃NO₄ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | Room temperature |
Product Description:
Used in solid-phase peptide synthesis as a chiral building block for introducing allyl-containing side chains. The Fmoc group allows for mild base deprotection, compatible with standard peptide synthesis protocols. The terminal alkene in the pentenyl side chain serves as a handle for post-assembly modifications, such as cross-metathesis or thiol-ene reactions, enabling peptide functionalization or conjugation to surfaces, tags, or other biomolecules. Its (R)-configuration supports studies on stereochemical effects in peptide structure and activity. Commonly applied in the development of bioconjugates, cyclic peptides, and peptide-based materials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | ฿1,880.00 |
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| 250mg | 10-20 days | ฿6,040.00 |
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| 1g | 10-20 days | ฿17,760.00 |
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(R)-N-Fmoc-2-(4'-pentenyl)glycine
Used in solid-phase peptide synthesis as a chiral building block for introducing allyl-containing side chains. The Fmoc group allows for mild base deprotection, compatible with standard peptide synthesis protocols. The terminal alkene in the pentenyl side chain serves as a handle for post-assembly modifications, such as cross-metathesis or thiol-ene reactions, enabling peptide functionalization or conjugation to surfaces, tags, or other biomolecules. Its (R)-configuration supports studies on stereochemical effects in peptide structure and activity. Commonly applied in the development of bioconjugates, cyclic peptides, and peptide-based materials.
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