(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(p-tolyl)butanoic acid
97%
- Product Code: 104339
CAS:
1260587-57-2
| Molecular Weight: | 415.48 g./mol | Molecular Formula: | C₂₆H₂₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07372120 | |
| 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 peptides, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality. This allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise assembly of peptide chains. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research in biochemistry and molecular biology. The p-tolyl group adds specific structural characteristics, which can be valuable in designing peptides with tailored properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿4,122.00 |
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| 0.100 | 10-20 days | ฿4,950.00 |
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| 0.250 | 10-20 days | ฿10,620.00 |
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| 1.000 | 10-20 days | ฿37,980.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(p-tolyl)butanoic acid
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality. This allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise assembly of peptide chains. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research in biochemistry and molecular biology. The p-tolyl group adds specific structural characteristics, which can be valuable in designing peptides with tailored properties.
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