PI12500 (1R,2R)-2-Benzylamino-1-cyclohexanol (CAS No.: 141553-09-5)

(1R,2R)-2-Benzylamino-1-cyclohexanol Description

(1R,2R)-2-Benzylamino-1-cyclohexanol is a chiral organic intermediate used in various chemical synthesis routes. Its precise molecular formula, C13H19NO, ensures consistency in reaction outcomes when incorporated into complex synthesis schemes. The powder form facilitates accurate weighing and handling, making it suitable for scale-up processes and mechanistic studies. This compound provides a defined stereocenter that benefits reactions requiring selectivity and predictable product distributions.

(1R,2R)-2-Benzylamino-1-cyclohexanol Applications

1.       Pharmaceutical Synthesis
- Used as a chiral building block in the synthesis of active pharmaceutical ingredients to achieve enantioselective reactions by leveraging its defined stereochemistry.
- Applied as an intermediate in the formation of key molecular scaffolds to improve reaction specificity and yield.

2.       Organic Research and Development
- Serves as a reagent in asymmetric synthesis protocols in academic and industrial laboratories to enhance reaction control by utilising its chiral properties.
- Frequently used in method development to test new synthetic pathways where controlled reactivity is critical.

(1R,2R)-2-Benzylamino-1-cyclohexanol Packing

The compound is packaged in moisture-proof, sealed containers with inert gas purging to reduce oxidation and contamination. Secondary packaging includes rigid protective casings to prevent physical damage during transport. Storage conditions require a cool, dry area away from direct sunlight. Custom packaging design options, including labelling and batch segregation, are available to accommodate specific handling requirements.

Additional Information

Chemical synthesis often relies on compounds with exact stereochemical configurations to drive selective reaction pathways. The study of chiral intermediates, such as (1R,2R)-2-Benzylamino-1-cyclohexanol, provides insights into asymmetric catalysis and reaction mechanism optimisation. Advances in analytical techniques support the rigorous characterisation of such compounds, enhancing reproducibility in synthetic processes.

Understanding the interplay between molecular structure and reactivity is critical in materials science and organic synthesis. The role of precision in stereochemical isomerism contributes to the efficient formation of high-value products in pharmaceuticals and speciality chemicals.