Perfluorophenyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)acetate
95%
- Product Code: 105456
CAS:
159631-29-5
| Molecular Weight: | 477.38 g./mol | Molecular Formula: | C₂₄H₁₆F₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 549.5±50.0 °C(Predicted) | |
| Density: | 1.434±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
Perfluorophenyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)acetate is widely utilized in peptide synthesis, particularly as an activated ester for coupling reactions. Its perfluorophenyl group enhances reactivity, making it effective for forming amide bonds with amino acids or peptides. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for amines, allowing selective deprotection during stepwise peptide assembly. This compound is especially valuable in solid-phase peptide synthesis (SPPS), where it ensures high coupling efficiency and minimizes side reactions. Its application extends to the preparation of complex peptides and peptide-based pharmaceuticals, contributing to advancements in drug development and biochemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,050.00 |
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| 1.000 | 10-20 days | ฿8,982.00 |
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| 5.000 | 10-20 days | ฿17,982.00 |
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Perfluorophenyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)acetate
Perfluorophenyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)acetate is widely utilized in peptide synthesis, particularly as an activated ester for coupling reactions. Its perfluorophenyl group enhances reactivity, making it effective for forming amide bonds with amino acids or peptides. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for amines, allowing selective deprotection during stepwise peptide assembly. This compound is especially valuable in solid-phase peptide synthesis (SPPS), where it ensures high coupling efficiency and minimizes side reactions. Its application extends to the preparation of complex peptides and peptide-based pharmaceuticals, contributing to advancements in drug development and biochemical research.
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