(S)-2-Amino-3-(3-chloro-2-fluorophenyl)propanoic acid hydrochloride
95%
- Product Code: 38259
CAS:
2375248-68-1
| Molecular Weight: | 254.0856 g./mol | Molecular Formula: | C₉H₁₀Cl₂FNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31706595 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its structural features, including the chloro and fluoro substituents on the phenyl ring, make it a valuable building block for designing drugs with enhanced specificity and potency. Researchers often employ it in the creation of compounds that interact with neurotransmitter systems, potentially leading to treatments for conditions such as depression, anxiety, or cognitive impairments. Additionally, its chiral nature allows for the exploration of stereospecific interactions in drug-receptor binding, contributing to the development of more effective and targeted therapies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $584.98 |
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(S)-2-Amino-3-(3-chloro-2-fluorophenyl)propanoic acid hydrochloride
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its structural features, including the chloro and fluoro substituents on the phenyl ring, make it a valuable building block for designing drugs with enhanced specificity and potency. Researchers often employ it in the creation of compounds that interact with neurotransmitter systems, potentially leading to treatments for conditions such as depression, anxiety, or cognitive impairments. Additionally, its chiral nature allows for the exploration of stereospecific interactions in drug-receptor binding, contributing to the development of more effective and targeted therapies.
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