2-(Iodomethyl)oxetane is a chemical compound characterized by its oxetane ring, which is a four-membered cyclic ether. The presence of the iodomethyl group at the 2-position of the oxetane ring introduces significant reactivity due to the electronegative iodine atom, which can participate in nucleophilic substitution reactions. This compound is typically a colorless to pale yellow liquid and is known for its potential applications in organic synthesis, particularly in the formation of more complex molecules. Its structure allows for various chemical transformations, making it a useful intermediate in the synthesis of pharmaceuticals and other organic compounds. Additionally, the presence of the iodine atom can enhance the compound's reactivity in coupling reactions or as a leaving group in nucleophilic attacks. Safety considerations should be taken into account when handling this compound, as iodine-containing substances can pose health risks. Overall, 2-(Iodomethyl)oxetane is a versatile building block in synthetic organic chemistry.

2-(Iodomethyl)oxetane

2-(Iodomethyl)oxetane is a carboxylic acid that can be synthesized in two steps from 2-iodoethanol. It is a useful reagent for the synthesis of unsaturated compounds, such as carboxylic acids, isoxazolines, and ethers. This compound can also be used as a starting material for the synthesis of other compounds with unsaturated bonds. 2-(Iodomethyl)oxetane reacts with nucleophiles to form oxetanes by way of intramolecular reactions. This reaction occurs at room temperature and does not require any catalysts or solvents. The reaction product is a mixture of diastereomers that can be separated by crystallization or chromatography.

CAS 121138-00-9: 2-(Iodomethyl)oxetane

2-(Iodomethyl)oxetane

Ref: IN-DA0080O6

2-(Iodomethyl)oxetane

Ref: 3D-WEA13800

2-Iodomethyloxetane

Ref: 54-OR309082

2-(Iodomethyl)oxetane

Ref: 10-F328670