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CAS 7149-90-8

:

2,4-dimethoxy-6-methylbenzaldehyde

Description:
2,4-Dimethoxy-6-methylbenzaldehyde, with the CAS number 7149-90-8, is an organic compound belonging to the class of aromatic aldehydes. It features a benzene ring substituted with two methoxy groups at the 2 and 4 positions, a methyl group at the 6 position, and an aldehyde functional group at the 1 position. This compound is typically characterized by its pleasant aromatic odor, which is often utilized in the fragrance industry. It is a colorless to pale yellow liquid at room temperature and 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 aldehyde group makes it reactive, particularly in condensation reactions and nucleophilic additions. Additionally, the methoxy groups can influence its reactivity and stability, often enhancing its electron-donating properties. Safety precautions should be taken when handling this compound, as with many organic chemicals, due to potential irritant effects and toxicity.
Formula:C10H12O3
InChI:InChI=1/C10H12O3/c1-7-4-8(12-2)5-10(13-3)9(7)6-11/h4-6H,1-3H3
SMILES:Cc1cc(cc(c1C=O)OC)OC
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Found 4 products.
  • 2,4-Dimethoxy-6-methylbenzaldehyde

    CAS:
    Formula:C10H12O3
    Purity:97%
    Molecular weight:180.2005

    Ref: IN-DA003FTJ

    1g
    111.00€
    5g
    263.00€
    100mg
    50.00€
    250mg
    65.00€
  • 2,4-Dimethoxy-6-methylbenzaldehyde

    CAS:
    2,4-Dimethoxy-6-methylbenzaldehyde
    Purity:98%

    Ref: 54-OR22049

    1g
    To inquire
    5g
    To inquire
    25g
    To inquire
    250mg
    51.00€
  • 2,4-Dimethoxy-6-methylbenzaldehyde

    CAS:
    2,4-Dimethoxy-6-methylbenzaldehyde is a biomolecular that belongs to the class of depsidones. It is a tetracyclic compound that has been isolated from the fungus Antrodia camphorata and the lichen Xanthoria polycarpa. 2,4-Dimethoxy-6-methylbenzaldehyde has been shown to inhibit the growth of fungi by preventing oxidative phosphorylation in mitochondria. This compound also shows regioselectivity for phenanthrenes, which are aromatic hydrocarbons with two benzene rings and one or more methyl groups on each ring. The synthesis of 2,4-dimethoxy-6-methylbenzaldehyde is achieved through a Witting reaction between olefinic compounds and diethyl malonate in the presence of base. 2,4-Dimethoxy-6-methylbenzaldehyde can also be synthesized by oxidizing dib
    Formula:C10H12O3
    Purity:Min. 95%
    Color and Shape:Powder
    Molecular weight:180.2 g/mol

    Ref: 3D-FD66741

    5g
    218.00€
  • 2,4-Dimethoxy-6-methylbenzaldehyde

    CAS:
    Purity:97%
    Molecular weight:180.2030029

    Ref: 10-F645913

    1g
    83.00€
    5g
    195.00€
    10g
    246.00€