Ethyl 2-(((1R,2S)-2-hydroxy-1,2-diphenylethyl)amino)acetate
≥95%
- Product Code: 41113
CAS:
112835-62-8
| Molecular Weight: | 299.36 g./mol | Molecular Formula: | C₁₈H₂₁NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09750955 | |
| Melting Point: | Boiling Point: | 436°C at 760 mmHg | |
| Density: | 1.15g/cm3 | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the synthesis of chiral molecules, particularly in the pharmaceutical industry, where it serves as a key intermediate for producing enantiomerically pure drugs. Its chiral structure makes it valuable in asymmetric synthesis, enabling the creation of compounds with high stereochemical precision. Additionally, it is employed in the development of catalysts for organic reactions, enhancing the efficiency and selectivity of processes like hydrogenation and C-C bond formation. In research, it is used to study stereochemical effects and to design novel bioactive molecules with potential therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | £111.95 |
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| 1.000 | 10-20 days | £223.91 |
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Ethyl 2-(((1R,2S)-2-hydroxy-1,2-diphenylethyl)amino)acetate
This compound is primarily utilized in the synthesis of chiral molecules, particularly in the pharmaceutical industry, where it serves as a key intermediate for producing enantiomerically pure drugs. Its chiral structure makes it valuable in asymmetric synthesis, enabling the creation of compounds with high stereochemical precision. Additionally, it is employed in the development of catalysts for organic reactions, enhancing the efficiency and selectivity of processes like hydrogenation and C-C bond formation. In research, it is used to study stereochemical effects and to design novel bioactive molecules with potential therapeutic applications.
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