(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(perfluorophenyl)butanoic acid
98%
- Product Code: 113767
CAS:
270063-43-9
| Molecular Weight: | 491.41 g./mol | Molecular Formula: | C₂₅H₁₈F₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861039 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in peptide synthesis as a building block for creating complex peptide structures. Its fluorenylmethoxycarbonyl (Fmoc) protecting group is particularly valuable in solid-phase peptide synthesis, allowing for the selective deprotection and coupling of amino acids. The perfluorophenyl group enhances its reactivity, making it useful in the formation of peptide bonds under mild conditions. Additionally, its unique structure can be employed in the development of fluorinated peptides, which are of interest in medicinal chemistry for their potential to improve metabolic stability and bioavailability. The compound is also explored in the design of peptide-based materials and bioconjugates, where its fluorinated moiety can impart specific properties such as increased hydrophobicity or resistance to degradation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,500.00 |
+
-
|
| 0.250 | 10-20 days | ฿6,336.00 |
+
-
|
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(perfluorophenyl)butanoic acid
This chemical is primarily utilized in peptide synthesis as a building block for creating complex peptide structures. Its fluorenylmethoxycarbonyl (Fmoc) protecting group is particularly valuable in solid-phase peptide synthesis, allowing for the selective deprotection and coupling of amino acids. The perfluorophenyl group enhances its reactivity, making it useful in the formation of peptide bonds under mild conditions. Additionally, its unique structure can be employed in the development of fluorinated peptides, which are of interest in medicinal chemistry for their potential to improve metabolic stability and bioavailability. The compound is also explored in the design of peptide-based materials and bioconjugates, where its fluorinated moiety can impart specific properties such as increased hydrophobicity or resistance to degradation.
| 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 :