(R)-2-((3-(Trifluoromethyl)phenoxy)methyl)oxirane, identified by its CAS number 124679-15-8, is an organic compound characterized by the presence of an epoxide functional group, which is a three-membered cyclic ether. The trifluoromethyl group attached to the phenoxy moiety enhances the compound's lipophilicity and may influence its reactivity and biological activity. The stereochemistry indicated by the (R) configuration suggests that the compound exhibits chirality, which can significantly affect its pharmacological properties and interactions with biological targets. This compound is likely to be of interest in medicinal chemistry and materials science due to its unique structural features. Its reactivity as an epoxide allows for potential applications in polymer synthesis and as an intermediate in organic synthesis. Additionally, the trifluoromethyl group can impart unique electronic properties, making it a valuable building block in the development of agrochemicals and pharmaceuticals. Safety and handling considerations should be taken into account due to the presence of fluorinated groups, which can pose environmental and health risks.

(R)-2-((3-(TRIFLUOROMETHYL)PHENOXY)METHYL)OXIRANE

124679-15-8: (R)-2-((3-(Trifluoromethyl)phenoxy)methyl)oxirane, identified by its CAS number 124679-15-8, is an organic compound characterized by the presence of an epoxide functional group, which is a three-membered cyclic ether. The trifluoromethyl group attached to the phenoxy moiety enhances the compound's lipophilicity and may influence its reactivity and biological activity. The stereochemistry indicated by the (R) configuration suggests that the compound exhibits chirality, which can significantly affect its pharmacological properties and interactions with biological targets. This compound is likely to be of interest in medicinal chemistry and materials science due to its unique structural features. Its reactivity as an epoxide allows for potential applications in polymer synthesis and as an intermediate in organic synthesis. Additionally, the trifluoromethyl group can impart unique electronic properties, making it a valuable building block in the development of agrochemicals and pharmaceuticals. Safety and handling considerations should be taken into account due to the presence of fluorinated groups, which can pose environmental and health risks.

CAS 124679-15-8

(R)-2-((3-(TRIFLUOROMETHYL)PHENOXY)METHYL)OXIRANE

Oxirane,[[3-(trifluoromethyl)phenoxy]methyl]-, (R)- (9CI)

Ref: IN-DA000MMG