(S)-3-Amino-4-(2-bromophenyl)butanoic acid hydrochloride
98%
- Product Code: 113794
CAS:
403661-76-7
| Molecular Weight: | 294.57 g./mol | Molecular Formula: | C₁₀H₁₃BrClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03093608 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a chiral center and a bromophenyl group, makes it valuable for the development of pharmaceutical agents, particularly those targeting neurological disorders. It is often employed in the preparation of compounds that act on neurotransmitter systems, such as GABA analogs, which are used to treat conditions like epilepsy, anxiety, and chronic pain. Additionally, its bromophenyl moiety can facilitate further chemical modifications, enabling the creation of diverse derivatives for drug discovery and optimization. Its hydrochloride form ensures stability and solubility, making it suitable for use in laboratory and industrial settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,828.00 |
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| 0.250 | 10-20 days | ฿14,724.00 |
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| 1.000 | 10-20 days | ฿36,693.00 |
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(S)-3-Amino-4-(2-bromophenyl)butanoic acid hydrochloride
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a chiral center and a bromophenyl group, makes it valuable for the development of pharmaceutical agents, particularly those targeting neurological disorders. It is often employed in the preparation of compounds that act on neurotransmitter systems, such as GABA analogs, which are used to treat conditions like epilepsy, anxiety, and chronic pain. Additionally, its bromophenyl moiety can facilitate further chemical modifications, enabling the creation of diverse derivatives for drug discovery and optimization. Its hydrochloride form ensures stability and solubility, making it suitable for use in laboratory and industrial settings.
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