(S)-1-(4-Bromo-3-chlorophenyl)ethanamine hydrochloride
≥95%
- Product Code: 235697
CAS:
1810074-64-6
| Molecular Weight: | 270.98 g./mol | Molecular Formula: | C₈H₁₀BrCl₂N |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26553540 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry seal |
Product Description:
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring enantiomeric purity. Its structure contains both bromo and chloro substituents, enabling further functionalization through cross-coupling reactions such as Suzuki or Heck reactions. The amine group allows for amide bond formation or conversion into heterocycles, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in research settings for the preparation of bioactive compounds, including potential central nervous system agents and anti-inflammatory drugs. The hydrochloride salt form enhances stability and solubility, facilitating handling and purification during synthetic processes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $441.41 |
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| 0.250 | 10-20 days | $751.23 |
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(S)-1-(4-Bromo-3-chlorophenyl)ethanamine hydrochloride
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring enantiomeric purity. Its structure contains both bromo and chloro substituents, enabling further functionalization through cross-coupling reactions such as Suzuki or Heck reactions. The amine group allows for amide bond formation or conversion into heterocycles, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in research settings for the preparation of bioactive compounds, including potential central nervous system agents and anti-inflammatory drugs. The hydrochloride salt form enhances stability and solubility, facilitating handling and purification during synthetic processes.
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