CAS 13246-46-3
:Benzaldehyde, 2,4-bis(phenylmethoxy)-
Description:
Benzaldehyde, 2,4-bis(phenylmethoxy)-, also known by its CAS number 13246-46-3, is an organic compound characterized by its structure, which features a benzaldehyde moiety substituted with two phenylmethoxy groups at the 2 and 4 positions. This compound typically exhibits a pale yellow to colorless appearance and has a distinctive aromatic odor, characteristic of benzaldehyde derivatives. It is generally soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. The presence of the methoxy groups enhances its stability and may influence its reactivity, making it useful in various chemical applications, including as an intermediate in organic synthesis and in the formulation of fragrances. Additionally, its aromatic structure suggests potential applications in materials science and as a building block in the synthesis of more complex organic molecules. Safety data should be consulted for handling and exposure guidelines, as with all chemical substances.
Formula:C21H18O3
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Found 4 products.
Benzaldehyde, 2,4-bis(phenylmethoxy)-
CAS:Formula:C21H18O3Purity:97%Color and Shape:SolidMolecular weight:318.36582,4-Dibenzyloxy benzaldehyde
CAS:<p>2,4-Dibenzyloxy benzaldehyde</p>Purity:96%Molecular weight:318.37g/mol2,4-bis(benzyloxy)benzaldehyde
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:318.372009277343752,4-Bis(benzyloxy)benzaldehyde
CAS:<p>2,4-Bis(benzyloxy)benzaldehyde is a prenylated aromatic compound that has been shown to have potent tyrosinase inhibitory activity. This effect was seen in murine melanoma cells and was found to be reversible. 2,4-Bis(benzyloxy)benzaldehyde also showed an inhibitory effect on the production of phytoalexins in plants. When combined with hydrochloric acid, 2,4-Bis(benzyloxy)benzaldehyde inhibits tyrosinase activity by interacting with the chloride ion on the enzyme's active site.</p>Formula:C21H18O3Purity:Min. 95%Molecular weight:318.37 g/mol




