Ethyl (R)-[(1-Phenylethyl)amino]acetate
≥97%
- Product Code: 76157
CAS:
66512-37-6
| Molecular Weight: | 207.27 g./mol | Molecular Formula: | C₁₂H₁₇NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06797321 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the preparation of various pharmaceutical compounds. Its structure, containing both an ester and an amine functional group, makes it a versatile intermediate in the synthesis of enantiomerically pure substances. It is particularly valuable in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry to achieve desired biological activity. Additionally, it can be employed in the development of asymmetric catalysts, which are crucial for creating chiral molecules in a more efficient and selective manner. Its application extends to research and development in medicinal chemistry, where it aids in the design and synthesis of novel drug candidates with improved efficacy and reduced side effects.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Pale yellow Crystal liquid |
| PURITY | 97-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿4,500.00 |
+
-
|
| 5.000 | 10-20 days | ฿11,660.00 |
+
-
|
Ethyl (R)-[(1-Phenylethyl)amino]acetate
This chemical is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the preparation of various pharmaceutical compounds. Its structure, containing both an ester and an amine functional group, makes it a versatile intermediate in the synthesis of enantiomerically pure substances. It is particularly valuable in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry to achieve desired biological activity. Additionally, it can be employed in the development of asymmetric catalysts, which are crucial for creating chiral molecules in a more efficient and selective manner. Its application extends to research and development in medicinal chemistry, where it aids in the design and synthesis of novel drug candidates with improved efficacy and reduced side effects.
| 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 :