(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid
98%
- Product Code: 38023
CAS:
204058-25-3
| Molecular Weight: | 494.5800 g./mol | Molecular Formula: | C₂₈H₃₄N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01321423 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptides and proteins, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group, while the tert-butoxycarbonyl (Boc) group shields the piperidine nitrogen, ensuring selective reactions during peptide chain assembly. Its structure allows for the introduction of piperidine-containing motifs into peptides, which are often explored in drug development for their potential bioactivity. After synthesis, the protecting groups can be removed under specific conditions to yield the desired peptide sequence. This compound is particularly valuable in pharmaceutical research for creating peptide-based therapeutics and studying biological interactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,438.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptides and proteins, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group, while the tert-butoxycarbonyl (Boc) group shields the piperidine nitrogen, ensuring selective reactions during peptide chain assembly. Its structure allows for the introduction of piperidine-containing motifs into peptides, which are often explored in drug development for their potential bioactivity. After synthesis, the protecting groups can be removed under specific conditions to yield the desired peptide sequence. This compound is particularly valuable in pharmaceutical research for creating peptide-based therapeutics and studying biological interactions.
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