(S)-2-Amino-3-(4-chlorophenyl)propan-1-ol hydrochloride
≥95%
- Product Code: 73176
CAS:
1956434-75-5
| Molecular Weight: | 222.11 g./mol | Molecular Formula: | C₉H₁₃Cl₂NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11618012 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily utilized in the synthesis of various pharmaceutical agents due to its chiral structure and functional groups. It serves as a key intermediate in the production of beta-blockers, which are medications used to manage cardiovascular conditions such as hypertension, arrhythmias, and angina. The presence of the chlorophenyl group enhances its binding affinity to specific receptors, making it valuable in drug development. Additionally, its hydrochloride form improves solubility, facilitating easier formulation into medicinal products. Researchers also explore its potential in creating novel therapeutic compounds targeting neurological disorders, leveraging its structural properties for enhanced efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft118,008.80 |
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| 0.250 | 10-20 days | Ft177,158.66 |
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(S)-2-Amino-3-(4-chlorophenyl)propan-1-ol hydrochloride
This compound is primarily utilized in the synthesis of various pharmaceutical agents due to its chiral structure and functional groups. It serves as a key intermediate in the production of beta-blockers, which are medications used to manage cardiovascular conditions such as hypertension, arrhythmias, and angina. The presence of the chlorophenyl group enhances its binding affinity to specific receptors, making it valuable in drug development. Additionally, its hydrochloride form improves solubility, facilitating easier formulation into medicinal products. Researchers also explore its potential in creating novel therapeutic compounds targeting neurological disorders, leveraging its structural properties for enhanced efficacy and selectivity.
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