(S)-1-(2,4-Dimethylphenyl)propan-1-amine hydrochloride
97%
- Product Code: 113623
CAS:
1032114-81-0
| Molecular Weight: | 199.72 g./mol | Molecular Formula: | C₁₁H₁₈ClN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12757588 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the production of more complex molecules. Its stereochemistry makes it particularly valuable in the development of pharmaceuticals, especially in the synthesis of enantiomerically pure drugs. The compound is often employed in the preparation of intermediates for active pharmaceutical ingredients (APIs) that require specific stereochemical configurations to achieve desired biological activity. Additionally, it finds use in research settings for studying asymmetric synthesis and catalysis, aiding in the development of more efficient and selective synthetic routes. Its hydrochloride form enhances stability and solubility, making it easier to handle in various chemical processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft73,307.03 |
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| 0.250 | 10-20 days | Ft146,711.03 |
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(S)-1-(2,4-Dimethylphenyl)propan-1-amine hydrochloride
This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block for the production of more complex molecules. Its stereochemistry makes it particularly valuable in the development of pharmaceuticals, especially in the synthesis of enantiomerically pure drugs. The compound is often employed in the preparation of intermediates for active pharmaceutical ingredients (APIs) that require specific stereochemical configurations to achieve desired biological activity. Additionally, it finds use in research settings for studying asymmetric synthesis and catalysis, aiding in the development of more efficient and selective synthetic routes. Its hydrochloride form enhances stability and solubility, making it easier to handle in various chemical processes.
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