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  • PI12672 (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol (CAS No.: 127852-28-2)

    • PI12672 (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol (CAS No.: 127852-28-2)

    Catalogue Number PI12672
    CAS Number 127852-28-2
    Composition C10H8F6O
    Form Powder

    (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol is a chiral fluorinated alcohol employed in advanced chemical synthesis. Stanford Advanced Materials (SAM) utilises rigorous solvent-free purification and spectroscopic analysis to monitor the product's enantiomeric purity. Their systematic approach including NMR and HPLC quality checks ensures conformity to technical specifications. SAM's facilities allow precise control over the reaction conditions, yielding reproducible batches suitable for research and industrial synthesis.

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    FAQ

    How does the chirality of (R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethanol influence its reactivity in synthesis processes?

    The chirality influences stereoselective reactions, allowing for controlled synthesis of enantiomerically enriched compounds. This specificity can minimise by-product formation during asymmetric reactions and improve overall reaction efficiency. Contact us for detailed reaction conditions.

    What analytical methods are recommended to verify the purity of this compound?

    Techniques such as NMR, HPLC, and mass spectrometry are advised to confirm the compound’s purity and enantiomeric excess. These methods provide quantitative and structural verification, essential for subsequent chemical synthesis steps. Contact us for further instrumentation details.

    Can this compound be used in catalytic asymmetric synthesis?

    Yes, its chiral nature makes it suitable for use as a starting material in catalytic asymmetric synthesis. Its structural properties aid in achieving high stereoselectivity during the formation of new chiral centres. Contact us to discuss application-specific parameters.

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