Dimethyl 4,4-disulfanediyl(2S,2S)-bis(2-((tert-butoxycarbonyl)amino)butanoate)
97%
- Product Code: 104572
CAS:
144373-70-6
| Molecular Weight: | 496.64 g./mol | Molecular Formula: | C₂₀H₃₆N₂O₈S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31803853 | |
| Melting Point: | 100-102 °C | Boiling Point: | 603.3±55.0 °C(Predicted) |
| Density: | 1.185±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of peptide synthesis, where it serves as a key intermediate for the development of complex peptide structures. Its disulfide linkage and tert-butoxycarbonyl (Boc) protecting groups make it particularly valuable in creating peptides with specific disulfide bonds, which are crucial for the stability and biological activity of many proteins and therapeutic peptides. Additionally, the Boc groups can be selectively removed under mild acidic conditions, allowing for further functionalization and coupling reactions in multi-step peptide synthesis processes. This chemical is also employed in research focused on designing peptide-based drugs, vaccines, and biomaterials, where precise control over molecular structure is essential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $115.12 |
+
-
|
| 1.000 | 10-20 days | $287.42 |
+
-
|
| 5.000 | 10-20 days | $1,004.30 |
+
-
|
Dimethyl 4,4-disulfanediyl(2S,2S)-bis(2-((tert-butoxycarbonyl)amino)butanoate)
This compound is primarily utilized in the field of peptide synthesis, where it serves as a key intermediate for the development of complex peptide structures. Its disulfide linkage and tert-butoxycarbonyl (Boc) protecting groups make it particularly valuable in creating peptides with specific disulfide bonds, which are crucial for the stability and biological activity of many proteins and therapeutic peptides. Additionally, the Boc groups can be selectively removed under mild acidic conditions, allowing for further functionalization and coupling reactions in multi-step peptide synthesis processes. This chemical is also employed in research focused on designing peptide-based drugs, vaccines, and biomaterials, where precise control over molecular structure is essential.
| 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 :