(S)-2-((tert-Butoxycarbonyl)amino)-4-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl)amino)butanoic acid
97%
- Product Code: 38106
CAS:
1263045-50-6
| Molecular Weight: | 382.4500 g./mol | Molecular Formula: | C₁₉H₃₀N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of peptide synthesis and organic chemistry research. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during chemical reactions. The presence of the 4,4-dimethyl-2,6-dioxocyclohexylidene moiety provides additional stability and selectivity in synthesis processes. It is often employed in the preparation of complex peptides, enabling precise control over the sequence and structure of the final product. Additionally, its unique structure makes it valuable in the development of pharmaceuticals and bioactive compounds, particularly in designing molecules with specific biological activities. The compound’s protective groups can be selectively removed under mild conditions, allowing for efficient and targeted synthesis strategies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,572.00 |
+
-
|
(S)-2-((tert-Butoxycarbonyl)amino)-4-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl)amino)butanoic acid
This compound is primarily utilized in the field of peptide synthesis and organic chemistry research. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during chemical reactions. The presence of the 4,4-dimethyl-2,6-dioxocyclohexylidene moiety provides additional stability and selectivity in synthesis processes. It is often employed in the preparation of complex peptides, enabling precise control over the sequence and structure of the final product. Additionally, its unique structure makes it valuable in the development of pharmaceuticals and bioactive compounds, particularly in designing molecules with specific biological activities. The compound’s protective groups can be selectively removed under mild conditions, allowing for efficient and targeted synthesis strategies.
| 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 :