(S)-1-(2,6-Dimethoxyphenyl)ethanamine hydrochloride
≥95%
- Product Code: 113640
CAS:
1956437-80-1
| Molecular Weight: | 217.69 g./mol | Molecular Formula: | C₁₀H₁₆ClNO₂ |
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| EC Number: | MDL Number: | MFCD24424960 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
(S)-1-(2,6-Dimethoxyphenyl)ethanamine hydrochloride is primarily utilized in the field of medicinal chemistry as a chiral building block for the synthesis of various pharmaceutical compounds. Its enantiomeric purity makes it particularly valuable in the development of drugs that require specific stereochemistry for optimal biological activity. This compound is often employed in the preparation of intermediates for potential therapeutic agents, particularly in the areas of central nervous system (CNS) disorders and cardiovascular diseases. Additionally, it serves as a key reagent in asymmetric synthesis, enabling the creation of complex molecules with high enantioselectivity. Its application extends to research and development laboratories where it aids in the exploration of novel drug candidates and the optimization of existing pharmacological treatments.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft27,441.65 |
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| 0.250 | 10-20 days | Ft56,725.68 |
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(S)-1-(2,6-Dimethoxyphenyl)ethanamine hydrochloride
(S)-1-(2,6-Dimethoxyphenyl)ethanamine hydrochloride is primarily utilized in the field of medicinal chemistry as a chiral building block for the synthesis of various pharmaceutical compounds. Its enantiomeric purity makes it particularly valuable in the development of drugs that require specific stereochemistry for optimal biological activity. This compound is often employed in the preparation of intermediates for potential therapeutic agents, particularly in the areas of central nervous system (CNS) disorders and cardiovascular diseases. Additionally, it serves as a key reagent in asymmetric synthesis, enabling the creation of complex molecules with high enantioselectivity. Its application extends to research and development laboratories where it aids in the exploration of novel drug candidates and the optimization of existing pharmacological treatments.
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