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CAS 63909-38-6

:

trans-4-benzyloxy-3-methoxy-beta-nitro-styrene

Description:
Trans-4-benzyloxy-3-methoxy-beta-nitro-styrene is an organic compound characterized by its complex structure, which includes a styrene backbone substituted with a nitro group, a benzyloxy group, and a methoxy group. The "trans" configuration indicates that the substituents are positioned on opposite sides of the double bond, which can influence its reactivity and physical properties. This compound typically exhibits moderate solubility in organic solvents due to its hydrophobic aromatic rings and polar functional groups. The presence of the nitro group suggests potential for electrophilic reactions, while the methoxy and benzyloxy groups can participate in various chemical transformations, including nucleophilic substitutions. Additionally, the compound may exhibit interesting optical properties due to its conjugated system, making it a candidate for applications in organic electronics or as a precursor in synthetic chemistry. Safety data should be consulted for handling, as nitro compounds can be sensitive and potentially hazardous.
Formula:C16H15NO4
Synonyms:
  • trans-4-Benzyloxy-3-methoxy-beta-nitrostyrene
  • 4-Benzyloxy-3-methoxy-omega-nitrostyrene
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Found 2 products.
  • (E)-1-(Benzyloxy)-2-methoxy-4-(2-nitrovinyl)benzene

    CAS:
    Formula:C16H15NO4
    Color and Shape:Solid
    Molecular weight:285.2946

    Ref: IN-DA003KTE

    ne
    To inquire
  • trans-4-Benzyloxy-3-methoxy-beta-nitrostyrene

    CAS:
    <p>Trans-4-Benzyloxy-3-methoxy-beta-nitrostyrene is an oxime that can be used as a catalyst for the catalytic hydrogenation of nitroalkanes. It is also a precursor to pallimamine, which is used as a pharmaceutical agent and an experimental virucide. Trans-4-Benzyloxy-3-methoxy-beta-nitrostyrene is synthesized by coupling two indole carboxylic acid analogues in the presence of sodium hydroxide and potassium carbonate. The reaction yields trans-(4'-benzyloxy)-3'-methoxystyrene, which is then converted to the title compound with ammonium chloride and hydrochloric acid. This compound undergoes acidic hydrolysis to yield the title compound.</p>
    Formula:C16H15NO4
    Purity:Min. 95%
    Color and Shape:Powder
    Molecular weight:285.29 g/mol

    Ref: 3D-FB65968

    850mg
    128.00€