3-Amino-3-(2-chlorophenyl)propanoic acid
98%
- Product Code: 44884
CAS:
68208-20-8
| Molecular Weight: | 199.6300 g./mol | Molecular Formula: | C₉H₁₀ClNO₂ |
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| EC Number: | MDL Number: | MFCD01871299 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring both an amino group and a chlorophenyl moiety, makes it a valuable building block in medicinal chemistry. It is often employed in the production of compounds targeting central nervous system disorders, such as anticonvulsants or anxiolytics, due to its ability to interact with specific biological receptors. Additionally, it serves as a precursor in the synthesis of chiral molecules, where its stereochemistry is leveraged to create enantiomerically pure drugs. Its application extends to research settings, where it is used to study structure-activity relationships in drug design and optimization.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,260.00 |
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3-Amino-3-(2-chlorophenyl)propanoic acid
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring both an amino group and a chlorophenyl moiety, makes it a valuable building block in medicinal chemistry. It is often employed in the production of compounds targeting central nervous system disorders, such as anticonvulsants or anxiolytics, due to its ability to interact with specific biological receptors. Additionally, it serves as a precursor in the synthesis of chiral molecules, where its stereochemistry is leveraged to create enantiomerically pure drugs. Its application extends to research settings, where it is used to study structure-activity relationships in drug design and optimization.
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