(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2,4-dichlorophenyl)butanoic acid
95%
- Product Code: 50305
CAS:
269396-54-5
| Molecular Weight: | 470.34 g./mol | Molecular Formula: | C₂₅H₂₁Cl₂NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01860947 | |
| Melting Point: | Boiling Point: | 672.3°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in peptide synthesis, where it serves as a protected amino acid derivative. Its fluorenylmethoxycarbonyl (Fmoc) group is crucial for temporary protection of the amino group during the synthesis process, ensuring selective reactions at specific sites. The presence of the dichlorophenyl group enhances its stability and influences its reactivity, making it suitable for constructing complex peptide sequences. It is particularly valuable in the production of pharmaceuticals and bioactive peptides, where precise control over molecular structure is essential. Additionally, its application extends to research and development in organic chemistry, aiding in the study of peptide interactions and functions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,871.00 |
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| 0.250 | 10-20 days | ฿4,869.00 |
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| 1.000 | 10-20 days | ฿13,140.00 |
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2,4-dichlorophenyl)butanoic acid
This chemical is primarily utilized in peptide synthesis, where it serves as a protected amino acid derivative. Its fluorenylmethoxycarbonyl (Fmoc) group is crucial for temporary protection of the amino group during the synthesis process, ensuring selective reactions at specific sites. The presence of the dichlorophenyl group enhances its stability and influences its reactivity, making it suitable for constructing complex peptide sequences. It is particularly valuable in the production of pharmaceuticals and bioactive peptides, where precise control over molecular structure is essential. Additionally, its application extends to research and development in organic chemistry, aiding in the study of peptide interactions and functions.
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