(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2,4-dichlorophenyl)butanoic acid
≥95%
- Product Code: 52357
CAS:
270063-49-5
| Molecular Weight: | 470.34 g./mol | Molecular Formula: | C₂₅H₂₁Cl₂NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861045 | |
| Melting Point: | Boiling Point: | 672.3°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective moiety for the amine functionality, ensuring that the amino acid remains stable during the synthesis process. This is particularly important in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling steps are required to build the desired peptide sequence. The presence of the 2,4-dichlorophenyl group can impart specific properties to the peptide, such as enhanced binding affinity or stability, making it useful in the development of biologically active peptides or peptidomimetics. Its application is significant in pharmaceutical research, particularly in the design and synthesis of peptide-based drugs or probes for studying biological interactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £86.71 |
+
-
|
| 0.250 | 10-20 days | £138.42 |
+
-
|
| 1.000 | 10-20 days | £352.15 |
+
-
|
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2,4-dichlorophenyl)butanoic acid
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective moiety for the amine functionality, ensuring that the amino acid remains stable during the synthesis process. This is particularly important in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling steps are required to build the desired peptide sequence. The presence of the 2,4-dichlorophenyl group can impart specific properties to the peptide, such as enhanced binding affinity or stability, making it useful in the development of biologically active peptides or peptidomimetics. Its application is significant in pharmaceutical research, particularly in the design and synthesis of peptide-based drugs or probes for studying biological interactions.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
£0.00
£0.00
Total :