2,4-Dimethyl-1,3-dioxolane is a cyclic organic compound characterized by its dioxolane structure, which features a five-membered ring containing two oxygen atoms and three carbon atoms. This compound is typically colorless and has a pleasant, ether-like odor. It is a liquid at room temperature and is known for its relatively low boiling point and moderate solubility in water, making it useful as a solvent in various chemical reactions and processes. The presence of the two methyl groups at the 2 and 4 positions contributes to its stability and influences its reactivity, particularly in nucleophilic substitution reactions. Additionally, 2,4-Dimethyl-1,3-dioxolane is often utilized in organic synthesis and as an intermediate in the production of other chemical compounds. Safety data indicates that it should be handled with care, as it may pose health risks if inhaled or ingested, and appropriate safety measures should be taken during its use in laboratory or industrial settings.

2,4-Dimethyl-1,3-dioxolane

3390-12-3: (2S,4S)-2,4-dimethyl-1,3-dioxolane, 1,3-Dioxolane, 2,4-Dimethyl-, 222-221-3, Acetaldehyde cyclic propylene acetal, Propylene acetal, 2,4-Dimethyl-1,3-dioxolane,  2,4-Dimethyl-1,3-dioxolane

2,4-Dimethyl-1,3-dioxolane (cis- and trans- mixture)

2,4-Dimethyl-1,3-dioxolane is a reactive chemical that participates in the formation of ion-exchanges and other reactions. It is an intermediate in the production of chlorinated hydrocarbons, such as vinyl chloride. 2,4-Dimethyl-1,3-dioxolane also reacts with acetaldehyde to produce 2,5-dimethylhexanedione. This reaction proceeds by bond cleavage with acid catalyst and is reversibly catalyzed. The product of this reaction has been shown to be a carbohydrate with aluminium.

CAS 3390-12-3: 2,4-Dimethyl-1,3-dioxolane

2,4-Dimethyl-1,3-dioxolane (cis- and trans- mixture)

Ref: 3B-D5748

2,4-Dimethyl-1,3-dioxolane

Ref: 3D-FD35542

2,4-DIMETHYL, 1,3-DIOXALONE

Ref: IN-DA00CAB0