4-Methyl-1,3,2-dioxathiolane 2-oxide, with the CAS number 1469-73-4, is a heterocyclic organic compound characterized by its unique dioxathiolane structure, which includes a five-membered ring containing both sulfur and oxygen atoms. This compound is typically colorless to pale yellow in appearance and is known for its stability under standard conditions. It exhibits properties typical of dioxathiolanes, such as being a potential electrophile due to the presence of the sulfur atom, which can participate in various chemical reactions, including nucleophilic attacks. The presence of the methyl group contributes to its reactivity and solubility in organic solvents. Additionally, 4-methyl-1,3,2-dioxathiolane 2-oxide is often studied for its applications in organic synthesis and as a reagent in various chemical transformations. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, this compound is of interest in both academic and industrial chemistry for its unique structural features and reactivity.

4-methyl-1,3,2-dioxathiolane 2-oxide

1469-73-4: 1,2-Propylene glycol sulfite, NSC 44145, 1,3,2-Dioxathiolane, 4-methyl-, 2-oxide, 1,2-Propanediol, cyclic sulfite, Propylene sulfite

4-Methyl-1,3,2-dioxathiolane 2-oxide is an alkynyl pyrimidine compound. It has a structural formula of C6H4N3O2. 4-Methyl-1,3,2-dioxathiolane 2-oxide reacts with lithium to produce ethylene diamine and nitrogen atoms. The reaction products are then reacted with methyl ethyl carbonate in the presence of high salt and a carbonate electrolyte to form vinylene. The properties of 4-methyl-1,3,2-dioxathiolane 2-oxide can be measured using electrochemical impedance spectroscopy on an aliphatic hydrocarbon.

CAS 1469-73-4: 4-methyl-1,3,2-dioxathiolane 2-oxide

4-Methyl-1,3,2-dioxathiolane 2-Oxide

Ref: 3D-FM61301

4-Methyl-1,3,2-dioxathiolane 2-Oxide (mixture of isomers)

Ref: 3B-M2471

Propane-1,2-cyclic sulfite

Ref: 54-OR914378

1,3,2-Dioxathiolane, 4-methyl-, 2-oxide

Ref: IN-DA001EFJ