(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4,4-difluorobutanoic acid
96%
- Product Code: 236968
CAS:
467442-21-3
| Molecular Weight: | 361.34 g./mol | Molecular Formula: | C₁₉H₁₇F₂NO₄ |
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| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Widely used in peptide synthesis, this compound serves as a protected chiral amino acid building block. Its main application lies in the preparation of modified peptides where enhanced metabolic stability and conformational control are required. The difluorinated side chain influences peptide backbone geometry and improves bioavailability, making it valuable in the development of pharmaceutical agents. The Fmoc group allows for mild, base-labile protection during solid-phase synthesis, enabling stepwise assembly of complex peptides. It is particularly useful in research settings focused on structure-activity relationship studies of bioactive peptides.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,250.00 |
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| 0.250 | 10-20 days | ฿6,360.00 |
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| 1.000 | 10-20 days | ฿25,280.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4,4-difluorobutanoic acid
Widely used in peptide synthesis, this compound serves as a protected chiral amino acid building block. Its main application lies in the preparation of modified peptides where enhanced metabolic stability and conformational control are required. The difluorinated side chain influences peptide backbone geometry and improves bioavailability, making it valuable in the development of pharmaceutical agents. The Fmoc group allows for mild, base-labile protection during solid-phase synthesis, enabling stepwise assembly of complex peptides. It is particularly useful in research settings focused on structure-activity relationship studies of bioactive peptides.
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