α,4-Dimethylbenzeneacetaldehyde, also known as p-tolylacetaldehyde, is an organic compound characterized by its aromatic structure and aldehyde functional group. It features a benzene ring substituted with two methyl groups at the 1 and 4 positions, along with an acetaldehyde group. This compound typically appears as a colorless to pale yellow liquid with a distinctive odor, reminiscent of floral or sweet notes. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. α,4-Dimethylbenzeneacetaldehyde is primarily used in the synthesis of various fragrances and flavoring agents, as well as in the production of other chemical intermediates. Its reactivity is influenced by the aldehyde group, allowing it to participate in typical reactions of aldehydes, such as oxidation and condensation. Safety considerations include handling it in well-ventilated areas and using appropriate personal protective equipment, as it may cause irritation to the skin and eyes.

α,4-Dimethylbenzeneacetaldehyde

99-72-9: 2-(4-Methylphenyl)Propan-1-Ol, 2-(4-Methylphenyl)Propanal, 2-(4-Tolyl)propanal, 2-(p-Methylphenyl)propanal, 2-(p-Methylphenyl)propionaldehyde, 2-(p-Tolyl)propanal, 2-(p-Tolyl)propionaldehyde, Benzeneacetaldehyde, α,4-dimethyl-, Hydratropaldehyde, p-methyl-, P-Methylhydratropaldehyde, α,4-Dimethylbenzeneacetaldehyde

2-(4-Methylphenyl)propanal is an organic compound that is used as a solvent and is homogeneous. It is a benzoate with alkylation activity, which can be used in kinetic and catalysis applications. 2-(4-Methylphenyl)propanal has also been shown to be effective in the synthesis of ethylbenzene derivatives, such as esters and acetonitrile. The reactions are carried out under pressure and at high temperatures. This chemical has been tested for its ability to catalyze reactions of glycols and solvents.

CAS 99-72-9: α,4-Dimethylbenzeneacetaldehyde

2-(4-Methylphenyl)propanal

Ref: 3D-AAA09972

4-methylhydratropaldehyde

Ref: 7W-GK8164