(2S)-2-(Fmoc-amino)-5-hexynoic acid
98%
- Product Code: 57130
CAS:
942518-21-0
| Molecular Weight: | 349.38 g./mol | Molecular Formula: | C₂₁H₁₉NO₄ |
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| EC Number: | MDL Number: | MFCD11052899 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, dry, sealed |
Product Description:
This chemical is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for introducing alkyne functionalities into peptides, which can be further modified through click chemistry reactions. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protective group for the amino group, allowing selective deprotection during the synthesis process. Its alkyne moiety enables conjugation with azide-containing molecules, making it valuable in bioconjugation and the development of peptide-based probes, drugs, and biomaterials. Additionally, it is utilized in research involving peptide labeling, imaging, and the study of protein-protein interactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿22,860.00 |
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(2S)-2-(Fmoc-amino)-5-hexynoic acid
This chemical is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for introducing alkyne functionalities into peptides, which can be further modified through click chemistry reactions. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protective group for the amino group, allowing selective deprotection during the synthesis process. Its alkyne moiety enables conjugation with azide-containing molecules, making it valuable in bioconjugation and the development of peptide-based probes, drugs, and biomaterials. Additionally, it is utilized in research involving peptide labeling, imaging, and the study of protein-protein interactions.
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