2,2-bis(bromomethyl)-1,3-dioxolane is a chemical compound characterized by its unique structure, which includes a dioxolane ring and two bromomethyl groups attached to the same carbon atom. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its reactivity due to the presence of bromine atoms, which can participate in various chemical reactions, including nucleophilic substitutions. The dioxolane ring contributes to its stability and solubility in polar solvents. This compound is often used in organic synthesis, particularly in the preparation of more complex molecules, and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Safety precautions are essential when handling this substance, as it may pose health risks due to its brominated nature and potential toxicity. Proper storage and disposal methods should be followed to mitigate environmental impact and ensure safety in laboratory settings.

2,2-bis(bromomethyl)-1,3-dioxolane

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2,2-BIS(BROMOMETHYL)-1,3-DIOXOLANE

2,2-Bis(bromomethyl)-1,3-dioxolane is a carbamate that is used in the synthesis of glycols. It is a tertiary alcohol that reacts with ethylene to produce ethylene glycol and tert-butyl carbamate. The tertiary alcohol moiety of 2,2-Bis(bromomethyl)-1,3-dioxolane then reacts with cyclohexanone to form cyclized products such as tert-butyl esters. This process can be scaled up for industrial purposes.

CAS 20599-01-3: 2,2-bis(bromomethyl)-1,3-dioxolane

2,2-BIS(BROMOMETHYL)-1,3-DIOXOLANE

Ref: 10-F470686

2,2-Bis(bromomethyl)-1,3-dioxolane

Ref: 3D-VAA59901

2,2-Bis(broMoMethyl)-1,3-dioxolane

Ref: IN-DA00BJIB