PI12201 N-[(1R,2R)-2-Amino-1,2-diphenylethyl]-4-(trifluoromethyl)benzenesulfonamide (CAS No.: 1105576-13-3)

N-[(1R,2R)-2-Amino-1,2-diphenylethyl]-4-(trifluoromethyl)benzenesulfonamide Description

N-[(1R,2R)-2-Amino-1,2-diphenylethyl]-4-(trifluoromethyl)benzenesulfonamide (C21H19F3N2O2S) is an organic reagent in powder form that demonstrates defined stereochemistry and an electron-withdrawing trifluoromethyl group. The specified structure makes it suitable as an intermediate for complex chemical synthesis. Routine spectroscopic analysis confirms its purity and structural integrity, which is crucial for achieving predictable reactivity in advanced research applications.

N-[(1R,2R)-2-Amino-1,2-diphenylethyl]-4-(trifluoromethyl)benzenesulfonamide Applications

Chemical Synthesis
- Utilised as an intermediate in pharmaceutical synthesis to achieve chiral centre formation by leveraging its well-defined stereochemistry.
- Applied as a reagent in constructing complex organic molecules to control reaction pathways by utilising its electron-withdrawing properties.

Academic Research
- Employed as a model compound in mechanistic organic studies to elucidate reaction steps by leveraging its defined diphenylethyl structure.
- Utilised in the development of synthetic methodologies to optimise reaction selectivity through controlled reactivity.

N-[(1R,2R)-2-Amino-1,2-diphenylethyl]-4-(trifluoromethyl)benzenesulfonamide Packing

The compound is packaged in inert, airtight containers to minimise moisture exposure and contamination. Each unit is sealed within an anti-static bag and housed in a rigid secondary carton for additional protection. The packaging is designed to reduce handling damage and is available with custom labelling and configuration options. Storage in a cool, low-humidity environment is recommended to maintain product integrity.

Additional Information

Advancements in organic synthesis have increased the demand for reagents with specific stereochemical configurations and functional group reactivity. Compounds such as N-[(1R,2R)-2-Amino-1,2-diphenylethyl]-4-(trifluoromethyl)benzenesulfonamide serve as fundamental building blocks to explore novel synthetic routes and reaction mechanisms.

Research in this field often requires detailed analytical characterisation. Techniques including NMR, HPLC, and mass spectrometry are essential for ensuring that the compound meets the rigorous demands of current synthesis protocols. This information underscores the material's significance in both academic investigations and industrial research.