(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hept-6-ynoic acid
97%
- Product Code: 57132
CAS:
1097192-05-6
| Molecular Weight: | 363.41 g./mol | Molecular Formula: | C₂₂H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11052907 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily used in peptide synthesis as a building block. It acts as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group safeguards the amino functionality during the coupling process. The alkyne group at the terminal end of the molecule allows for further functionalization via click chemistry, enabling the attachment of various tags or probes. Its application is crucial in the development of peptide-based drugs, biomaterials, and bioconjugates, particularly in research involving targeted drug delivery and molecular imaging. The compound’s stability and reactivity make it a valuable tool in organic and medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿19,800.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hept-6-ynoic acid
This compound is primarily used in peptide synthesis as a building block. It acts as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group safeguards the amino functionality during the coupling process. The alkyne group at the terminal end of the molecule allows for further functionalization via click chemistry, enabling the attachment of various tags or probes. Its application is crucial in the development of peptide-based drugs, biomaterials, and bioconjugates, particularly in research involving targeted drug delivery and molecular imaging. The compound’s stability and reactivity make it a valuable tool in organic and medicinal chemistry.
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