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CAS 96156-72-8

:

(S)-(-)-1-(4-nitrophenyl)ethanol

Description:
(S)-(-)-1-(4-nitrophenyl)ethanol, with the CAS number 96156-72-8, is an organic compound characterized by its chiral structure, which includes a hydroxyl group (-OH) attached to a carbon atom that is also bonded to a 4-nitrophenyl group. This compound is a secondary alcohol, indicating that the hydroxyl group is attached to a carbon that is connected to two other carbon atoms. The presence of the nitrophenyl group introduces significant electron-withdrawing characteristics, which can influence the compound's reactivity and solubility. Typically, such compounds exhibit optical activity due to their chiral nature, allowing them to rotate plane-polarized light. (S)-(-)-1-(4-nitrophenyl)ethanol may be utilized in various applications, including as an intermediate in organic synthesis and in the development of pharmaceuticals. Its properties, such as boiling point, melting point, and solubility, can vary based on the specific conditions and solvents used. Overall, this compound is of interest in both academic research and industrial applications due to its unique structural features and potential reactivity.
Formula:C8H9NO3
Synonyms:
  • (S)-(+)-alpha-(p-Nitrophenyl)ethanol
  • Benzenemethanol, alpha-methyl-4-nitro-, (alphaS)- (9CI)
  • (S)-1-(p-Nitrophenyl)ethanol
  • Benzenemethanol, α-methyl-4-nitro-, (αS)-
  • (1S)-1-(4-nitrophenyl)ethan-1-ol
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Found 2 products.
  • CymitQuimica logo
    Apollo Scientific
    + Info

    (S)-1-(4-Nitrophenyl)ethan-1-ol

    CAS:
    (S)-1-(4-Nitrophenyl)ethan-1-ol
    Purity:95%
    Molecular weight:167.16g/mol

    Ref: 54-OR1075173

    1g
    275.00€
    5g
    662.00€
    10g
    1,097.00€
    25g
    1,837.00€
    100mg
    69.00€
    250mg
    114.00€
  • (1S)-1-(4-Nitrophenyl)ethan-1-ol
    Biosynth
    + Info

    (1S)-1-(4-Nitrophenyl)ethan-1-ol

    CAS:
    <p>(1S)-1-(4-Nitrophenyl)ethan-1-ol is an intermediate in the synthesis of a chiral alcohol. It can be prepared by hydrogenolysis of (1R)-1-phenylethanol with palladium on carbon, followed by catalytic reduction of the nitro group. The hydrogenolysis can also be carried out in the presence of lipase, which will produce a higher yield. This intermediate can then be used to synthesize other compounds, such as 4-nitroacetophenone and chiral alcohols.</p>
    Formula:C8H9NO3
    Purity:Min. 95%
    Color and Shape:Powder
    Molecular weight:167.16 g/mol

    Ref: 3D-WDA15672

    50mg
    437.00€
    500mg
    1,096.00€