2-[(2,6-Dimethoxyphenoxy)methyl]oxirane, with the CAS number 5435-29-0, is an organic compound characterized by its epoxide functional group, which is a three-membered cyclic ether. This compound features a phenoxy group substituted with two methoxy groups at the 2 and 6 positions of the aromatic ring, enhancing its reactivity and solubility in organic solvents. The presence of the oxirane ring contributes to its potential as a reactive intermediate in various chemical reactions, including ring-opening reactions that can lead to the formation of larger, more complex molecules. The methoxy substituents can influence the electronic properties of the molecule, potentially affecting its reactivity and interactions with other chemical species. Additionally, the compound may exhibit interesting biological activities, making it of interest in medicinal chemistry and material science. Its unique structure allows for diverse applications, including use in the synthesis of polymers, pharmaceuticals, and agrochemicals. Safety and handling precautions should be observed due to the reactive nature of the epoxide group.

2-[(2,6-dimethoxyphenoxy)methyl]oxirane

5435-29-0: 2-[(2,6-Dimethoxyphenoxy)methyl]oxirane, with the CAS number 5435-29-0, is an organic compound characterized by its epoxide functional group, which is a three-membered cyclic ether. This compound features a phenoxy group substituted with two methoxy groups at the 2 and 6 positions of the aromatic ring, enhancing its reactivity and solubility in organic solvents. The presence of the oxirane ring contributes to its potential as a reactive intermediate in various chemical reactions, including ring-opening reactions that can lead to the formation of larger, more complex molecules. The methoxy substituents can influence the electronic properties of the molecule, potentially affecting its reactivity and interactions with other chemical species. Additionally, the compound may exhibit interesting biological activities, making it of interest in medicinal chemistry and material science. Its unique structure allows for diverse applications, including use in the synthesis of polymers, pharmaceuticals, and agrochemicals. Safety and handling precautions should be observed due to the reactive nature of the epoxide group.

CAS 5435-29-0

2-[(2,6-dimethoxyphenoxy)methyl]oxirane

2-(2,6-Dimethoxyphenoxymethyl)oxirane

Ref: 3D-FAA43529