(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyl-3-phenylpropanoic acid
≥95%
- Product Code: 38019
CAS:
135944-05-7
| Molecular Weight: | 401.45 g./mol | Molecular Formula: | C₂₅H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02682285 | |
| Melting Point: | Boiling Point: | 621.2°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during the peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS), allowing for the stepwise construction of peptides with high precision. The compound’s structure, featuring a phenyl group and a methyl group, contributes to its stability and compatibility with various coupling reagents. After the peptide synthesis is complete, the Fmoc group can be easily removed under mild basic conditions, making it a versatile tool in the production of peptides for pharmaceutical and biochemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,008.00 |
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| 0.250 | 10-20 days | ฿1,764.00 |
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| 1.000 | 10-20 days | ฿4,401.00 |
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| 5.000 | 10-20 days | ฿19,071.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyl-3-phenylpropanoic acid
This chemical is primarily used in peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amino functionality, ensuring selective reactions during the peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis (SPPS), allowing for the stepwise construction of peptides with high precision. The compound’s structure, featuring a phenyl group and a methyl group, contributes to its stability and compatibility with various coupling reagents. After the peptide synthesis is complete, the Fmoc group can be easily removed under mild basic conditions, making it a versatile tool in the production of peptides for pharmaceutical and biochemical research.
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