(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-phenylpropanoic acid
≥95%
- Product Code: 54996
CAS:
1217722-24-1
| Molecular Weight: | 387.43 g./mol | Molecular Formula: | C₂₄H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11052914 | |
| Melting Point: | Boiling Point: | 619.0±50.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in peptide synthesis as a building block. It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group protects the amine functionality during the peptide chain assembly. This allows for selective deprotection and coupling of amino acids in solid-phase peptide synthesis (SPPS). Its phenyl group provides structural diversity, making it useful in synthesizing peptides with specific properties or biological activities. Additionally, it is employed in the development of pharmaceuticals and bioactive peptides, particularly in research focused on drug discovery and therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,980.00 |
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| 0.250 | 10-20 days | ฿17,550.00 |
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| 1.000 | 10-20 days | ฿43,929.00 |
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-phenylpropanoic acid
This chemical is primarily used in peptide synthesis as a building block. It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group protects the amine functionality during the peptide chain assembly. This allows for selective deprotection and coupling of amino acids in solid-phase peptide synthesis (SPPS). Its phenyl group provides structural diversity, making it useful in synthesizing peptides with specific properties or biological activities. Additionally, it is employed in the development of pharmaceuticals and bioactive peptides, particularly in research focused on drug discovery and therapeutic agents.
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