CAS 3207-04-3

Oxetane, 3-ethyl-3-[(2-propenyloxy)methyl]-

Description:

Oxetane, 3-ethyl-3-[(2-propenyloxy)methyl]- is a cyclic ether characterized by a four-membered ring structure containing an oxygen atom. This compound features an ethyl group and a propenyloxy methyl substituent, which contribute to its unique reactivity and properties. The presence of the oxetane ring imparts strain, making it more reactive than larger cyclic ethers. This compound is typically colorless and may have a faint odor. It is soluble in organic solvents, reflecting its non-polar characteristics, while its reactivity allows it to participate in various chemical reactions, including polymerization and ring-opening reactions. Oxetanes are of interest in synthetic organic chemistry and materials science due to their potential applications in the development of polymers and other functional materials. Safety data should be consulted for handling, as with many organic compounds, it may pose health risks if not managed properly. Overall, the unique structure and reactivity of 3-ethyl-3-[(2-propenyloxy)methyl]-oxetane make it a compound of interest in both academic and industrial chemistry.

Formula: C₉H₁₆O₂

3-[(Allyloxy)methyl]-3-ethyloxetane

CAS: 3207-04-3

Formula: C₉H₁₆O₂

Purity: 97%

Molecular weight: 156.2221

Ref: IN-DA01JRND

3-[(Allyloxy)methyl]-3-ethyloxetane

CAS: 3207-04-3

Formula: C₉H₁₆O₂

Purity: >98.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 156.23

Ref: 3B-A3362

3-[(Allyloxy)methyl]-3-ethyloxetane

CAS: 3207-04-3

3-[(Allyloxy)methyl]-3-ethyloxetane is a reactive chemical compound that is used in the synthesis of cationic polymers. 3-[(Allyloxy)methyl]-3-ethyloxetane has been shown to be able to form crosslinks with epoxide groups and form polymers. The ring-opening reactions are thermally reversible, and the oxetane morphologies can be classified as linear or cyclic. Protonation of this compound leads to the formation of carbocations, which are reactive intermediates that can react with other molecules. Compartmentalization of this compound leads to the formation of cations, which are positively charged species. Cationic polymerization is a technique in which 3-[(Allyloxy)methyl]-3-ethyloxetane is used as a monomer for the synthesis of polymers with cationic side chains.

Formula: C₉H₁₆O₂

Purity: Min. 95%

Molecular weight: 156.22 g/mol

Ref: 3D-DAA20704