(R)-Methyl 2-((tert-butoxycarbonyl)amino)-3-phenylpropanoate
98%
- Product Code: 53526
CAS:
77119-84-7
| Molecular Weight: | 279.33 g./mol | Molecular Formula: | C₁₅H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00672509 | |
| Melting Point: | Boiling Point: | 403.7±38.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in the synthesis of pharmaceuticals, particularly in the production of peptide-based drugs. It serves as a key intermediate in the preparation of chiral compounds, which are essential for creating enantiomerically pure active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide coupling reactions, where it helps in the stepwise assembly of amino acids without unwanted side reactions. Additionally, it is employed in organic synthesis for constructing complex molecules with specific stereochemistry, which is crucial in drug development and research. Its application extends to the study of enzyme inhibitors and receptor modulators, where precise molecular configuration is required for biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $24.07 |
+
-
|
| 1.000 | 10-20 days | $61.94 |
+
-
|
| 5.000 | 10-20 days | $246.34 |
+
-
|
| 10.000 | 10-20 days | $453.04 |
+
-
|
(R)-Methyl 2-((tert-butoxycarbonyl)amino)-3-phenylpropanoate
This chemical is primarily used in the synthesis of pharmaceuticals, particularly in the production of peptide-based drugs. It serves as a key intermediate in the preparation of chiral compounds, which are essential for creating enantiomerically pure active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide coupling reactions, where it helps in the stepwise assembly of amino acids without unwanted side reactions. Additionally, it is employed in organic synthesis for constructing complex molecules with specific stereochemistry, which is crucial in drug development and research. Its application extends to the study of enzyme inhibitors and receptor modulators, where precise molecular configuration is required for biological activity.
| 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 :