Fmoc-(S)-3-Amino-4-(3,4-dichloro-phenyl)-butyric acid
98%
- Product Code: 104985
CAS:
270063-52-0
| Molecular Weight: | 470.35 g./mol | Molecular Formula: | C₂₅H₂₁Cl₂NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861048 | |
| Melting Point: | Boiling Point: | 674.1±55.0 °C(Predicted) | |
| Density: | 1.367±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the peptide chain assembly. The presence of the dichlorophenyl group in its structure makes it valuable for introducing specific hydrophobic and aromatic characteristics into peptides, which can be crucial for biological activity or binding properties. It is often employed in the development of peptide-based drugs, research peptides, or bioactive compounds targeting specific receptors or enzymes. Its application is particularly relevant in medicinal chemistry and biochemistry for designing peptides with enhanced stability, specificity, or therapeutic potential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,322.00 |
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| 0.250 | 10-20 days | ฿3,735.00 |
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| 1.000 | 10-20 days | ฿7,461.00 |
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Fmoc-(S)-3-Amino-4-(3,4-dichloro-phenyl)-butyric acid
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the peptide chain assembly. The presence of the dichlorophenyl group in its structure makes it valuable for introducing specific hydrophobic and aromatic characteristics into peptides, which can be crucial for biological activity or binding properties. It is often employed in the development of peptide-based drugs, research peptides, or bioactive compounds targeting specific receptors or enzymes. Its application is particularly relevant in medicinal chemistry and biochemistry for designing peptides with enhanced stability, specificity, or therapeutic potential.
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