3-(3-Methoxyphenyl)-3-(trifluoromethyl)-diaziridine, identified by its CAS number 154187-45-8, is a diaziridine compound characterized by the presence of a diaziridine ring, which consists of two adjacent nitrogen atoms within a three-membered carbon ring. This compound features a methoxyphenyl group, contributing to its aromatic properties, and a trifluoromethyl group, which enhances its reactivity and lipophilicity due to the electronegative fluorine atoms. The presence of these functional groups suggests potential applications in medicinal chemistry and materials science, particularly in the development of pharmaceuticals or agrochemicals. The trifluoromethyl group can impart unique electronic properties, making the compound of interest for various synthetic pathways. Additionally, diaziridines are known for their ability to undergo ring-opening reactions, which can lead to the formation of diverse chemical entities. Overall, this compound's unique structural features and functional groups make it a subject of interest for further research and application in organic synthesis.

3-(3-METHOXYPHENYL)-3-(TRIFLUOROMETHYL)-DIAZIRIDINE

154187-45-8: 3-(3-Methoxyphenyl)-3-(trifluoromethyl)-diaziridine, identified by its CAS number 154187-45-8, is a diaziridine compound characterized by the presence of a diaziridine ring, which consists of two adjacent nitrogen atoms within a three-membered carbon ring. This compound features a methoxyphenyl group, contributing to its aromatic properties, and a trifluoromethyl group, which enhances its reactivity and lipophilicity due to the electronegative fluorine atoms. The presence of these functional groups suggests potential applications in medicinal chemistry and materials science, particularly in the development of pharmaceuticals or agrochemicals. The trifluoromethyl group can impart unique electronic properties, making the compound of interest for various synthetic pathways. Additionally, diaziridines are known for their ability to undergo ring-opening reactions, which can lead to the formation of diverse chemical entities. Overall, this compound's unique structural features and functional groups make it a subject of interest for further research and application in organic synthesis.

<p>Applications A photoaffinity reagent.<br>References Hatanaka, Y. et al: Bioorg. Med. Chem., 2, 1367 (1994); Hatanaka, Y. et al: J. Org. Chem., 59, 383 (1994); Hatanaka, Y. et al: Bioorg. Med. Chem. 2, 1367 (1994)<br></p>

CAS 154187-45-8

3-(3-METHOXYPHENYL)-3-(TRIFLUOROMETHYL)-DIAZIRIDINE

3-(3-Methoxyphenyl)-3-(trifluoromethyl)-diaziridine

Ref: TR-M266345