(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-oxo-4-(tritylamino)butanoic acid
≥95%
- Product Code: 50397
CAS:
941296-80-6
| Molecular Weight: | 610.70 g./mol | Molecular Formula: | C₃₉H₃₄N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22200773 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a key building block for the introduction of specific amino acid residues into peptide chains. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino function, ensuring selective reactions during the synthesis process. The trityl (Trt) group protects the amino side chain, allowing for controlled deprotection and modification. Its application is crucial in the production of complex peptides used in pharmaceutical research, drug development, and biochemical studies. Additionally, it aids in the synthesis of peptides with specific structural and functional properties, making it valuable in the development of therapeutic agents and biomaterials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,105.00 |
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| 1.000 | 10-20 days | ฿6,570.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-oxo-4-(tritylamino)butanoic acid
This chemical is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a key building block for the introduction of specific amino acid residues into peptide chains. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino function, ensuring selective reactions during the synthesis process. The trityl (Trt) group protects the amino side chain, allowing for controlled deprotection and modification. Its application is crucial in the production of complex peptides used in pharmaceutical research, drug development, and biochemical studies. Additionally, it aids in the synthesis of peptides with specific structural and functional properties, making it valuable in the development of therapeutic agents and biomaterials.
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