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Product Line: Pharmaceutical Chemicals

(S)-3-Amino-3-(4-chlorophenyl)propan-1-ol

CAS 886061-26-3

Molecular structure of (S)-3-Amino-3-(4-chlorophenyl)propan-1-ol

CAS · 886061-26-3

01

Product Overview

(S)-3-Amino-3-(4-chlorophenyl)propan-1-ol is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.

02

Product Specifications

Appearance White solid
Purity 98% min
Chiral purity 99% min
Water 1.0% max
Unknown single impurity 0.5% max
03

Applications

(S)-3-Amino-3-(4-chlorophenyl)propan-1-ol is primarily used as a chiral intermediate in the synthesis of pharmaceuticals, bioactive compounds, and specialty chemicals. It serves as a building block for the preparation of β-amino alcohol derivatives, which are important scaffolds in medicinal chemistry for the development of central nervous system agents, enzyme inhibitors, and receptor modulators. The compound is commonly applied in drug discovery research for constructing stereochemically defined molecules with specific biological activity. It is also used in the synthesis of chiral ligands and catalysts, where its amino and hydroxyl groups provide sites for functionalization and derivatization. Additionally, in research laboratories, it is employed to study reaction mechanisms, asymmetric synthesis, and structure–activity relationships in drug development.

04

Benefits

The benefits of (S)-3-Amino-3-(4-chlorophenyl)propan-1-ol arise from its high enantiomeric purity, multifunctional groups, and chemical stability. Its S-configuration allows the preparation of optically active compounds, which is critical in medicinal chemistry where stereochemistry strongly influences pharmacological activity. The combination of amino, hydroxyl, and chlorophenyl functionalities provides versatile reaction sites, enabling selective derivatization, coupling, and incorporation into complex molecules. Its stability under standard storage and reaction conditions ensures reproducible results in both laboratory and industrial applications. The compound's compatibility with common organic synthesis reagents and protecting-group strategies enhances efficiency, yields, and selectivity in multi-step synthetic pathways.

05

Conclusion

(S)-3-Amino-3-(4-chlorophenyl)propan-1-ol is a valuable chiral intermediate for pharmaceutical synthesis, bioactive compound development, and asymmetric chemical research. Its stereochemical purity, multifunctionality, and stability make it an important building block for creating optically active molecules and exploring structure–activity relationships, supporting both industrial applications and academic research in drug discovery.

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