(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(perfluorophenyl)butanoic acid
98%
- Product Code: 104972
CAS:
269398-94-9
| Molecular Weight: | 491.41 g./mol | Molecular Formula: | C₂₅H₁₈F₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01860941 | |
| Melting Point: | Boiling Point: | 616.7±55.0 °C(Predicted) | |
| Density: | 1.441±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of peptide synthesis, where it serves as a key building block for the creation of complex peptide structures. Its unique structure, featuring a fluorenylmethyloxycarbonyl (Fmoc) protecting group, allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise assembly of peptides with high precision. The perfluorophenyl group enhances the compound's stability and reactivity, making it particularly useful in the synthesis of peptides with specific functional properties. Additionally, it finds application in the development of pharmaceutical compounds, where its incorporation can improve the pharmacokinetic properties of drug candidates. Researchers also employ it in the study of protein interactions and enzyme mechanisms, leveraging its distinct chemical characteristics to probe biological systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,429.00 |
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| 0.250 | 10-20 days | ฿6,858.00 |
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| 1.000 | 10-20 days | ฿19,458.00 |
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(perfluorophenyl)butanoic acid
This chemical is primarily utilized in the field of peptide synthesis, where it serves as a key building block for the creation of complex peptide structures. Its unique structure, featuring a fluorenylmethyloxycarbonyl (Fmoc) protecting group, allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise assembly of peptides with high precision. The perfluorophenyl group enhances the compound's stability and reactivity, making it particularly useful in the synthesis of peptides with specific functional properties. Additionally, it finds application in the development of pharmaceutical compounds, where its incorporation can improve the pharmacokinetic properties of drug candidates. Researchers also employ it in the study of protein interactions and enzyme mechanisms, leveraging its distinct chemical characteristics to probe biological systems.
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