Methyl 2-Amino-2-(3,4-dichlorophenyl)acetate Hydrochloride
≥97%
- Product Code: 58291
CAS:
1078611-21-8
| Molecular Weight: | 270.54 g./mol | Molecular Formula: | C₉H₁₀Cl₃NO₂ |
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| EC Number: | MDL Number: | MFCD04115512 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily used in the synthesis of pharmaceutical agents, particularly in the development of drugs targeting the central nervous system. It serves as a key intermediate in the production of compounds with potential antidepressant or anxiolytic properties. Its structural features make it valuable for creating molecules that interact with specific neurotransmitter systems.
In research settings, it is utilized to study the structure-activity relationships of bioactive molecules, helping to optimize their efficacy and selectivity. Additionally, it may be employed in the preparation of chiral compounds, leveraging its stereochemistry for asymmetric synthesis. Its application is largely confined to laboratory-scale processes in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $323.76 |
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| 1.000 | 10-20 days | $764.72 |
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Methyl 2-Amino-2-(3,4-dichlorophenyl)acetate Hydrochloride
This compound is primarily used in the synthesis of pharmaceutical agents, particularly in the development of drugs targeting the central nervous system. It serves as a key intermediate in the production of compounds with potential antidepressant or anxiolytic properties. Its structural features make it valuable for creating molecules that interact with specific neurotransmitter systems.
In research settings, it is utilized to study the structure-activity relationships of bioactive molecules, helping to optimize their efficacy and selectivity. Additionally, it may be employed in the preparation of chiral compounds, leveraging its stereochemistry for asymmetric synthesis. Its application is largely confined to laboratory-scale processes in medicinal chemistry and drug discovery.
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