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CAS 93943-06-7

:

Benzaldehyde,4-(methoxymethyl)-

Description:
Benzaldehyde, 4-(methoxymethyl)-, also known by its CAS number 93943-06-7, is an organic compound characterized by the presence of a benzaldehyde group substituted with a methoxymethyl group at the para position. This compound typically appears as a colorless to pale yellow liquid with a sweet, almond-like odor, characteristic of benzaldehyde derivatives. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. The presence of the methoxymethyl group enhances its reactivity, making it a useful intermediate in organic synthesis, particularly in the production of various pharmaceuticals and agrochemicals. Additionally, it may exhibit biological activity, which can be explored for potential applications in medicinal chemistry. As with many aromatic compounds, it is important to handle this substance with care, as it may pose health risks if inhaled or ingested. Proper safety measures should be employed when working with this chemical in laboratory settings.
Formula:C9H10O2
Synonyms:
  • p-Tolualdehyde,a-methoxy- (6CI)
  • 4-(Methoxymethyl)benzaldehyde
  • p-(Methoxymethyl)benzaldehyde
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Found 3 products.
  • 4-(METHOXYMETHYL)-BENZALDEHYDE

    CAS:
    Formula:C9H10O2
    Purity:95%
    Color and Shape:Liquid
    Molecular weight:150.1745

    Ref: IN-DA00H74X

    1g
    692.00€
    5g
    To inquire
  • 4-(Methoxymethyl)benzaldehyde

    CAS:
    Formula:C9H10O2
    Purity:≥95%
    Color and Shape:Liquid, Oil
    Molecular weight:150.177

    Ref: 10-F396286

    1g
    646.00€
    5g
    1,777.00€
  • 4-(Methoxymethyl)benzaldehyde

    CAS:
    <p>4-(Methoxymethyl)benzaldehyde is an organic chemical compound that has the molecular formula CHO. It can be obtained by catalytic cleavage of 4-hydroxybenzaldehyde with hydrogen chloride in the presence of a nickel catalyst, followed by chlorination and reduction. This chemical is used in pharmaceuticals as a catalyst for reductive cleavage and cyclization reactions. The acidity of 4-(methoxymethyl)benzaldehyde is due to its nitrogen substituents, which are capable of deprotonating the carbon atom adjacent to the carbonyl group. This allows for selective synthesis at the benzylic position.<br>4-(Methoxymethyl)benzaldehyde is also able to catalyze lithiation reactions because it contains a reactive chlorine atom.</p>
    Formula:C9H10O2
    Purity:Min. 95%
    Molecular weight:150.17 g/mol

    Ref: 3D-TDA94306

    250mg
    386.00€
    2500mg
    1,383.00€