87964-46-3

Usage

Physical state

Colorless to pale yellow liquid

Usage

Building block in the synthesis of pharmaceutical and agrochemical products

Applications

a. Intermediate in the production of pharmaceuticals (antiviral, antibacterial, and antifungal drugs)
b. Key ingredient in the production of pesticides and herbicides

Isomer

cis-

Stability

High stability

Industrial applications

Widely utilized

Safety

Handle with caution due to potential hazards if not used properly

Upstream product

• 42136-65-2 cis-1-benzyl-2,3-diphenylaziridine 
• 58268-17-0 (Z)-1-butyl-2,3-diphenylaziridine 

Relevant academic research and scientific papers

FORMATION OF 1,2,4-DIOXAZOLIDINES BY ELECTRON-TRANSFER PHOTOOXYGENATION OF AZIRIDINES

DCA-sensitized photooxygenation of cis- and trans-2,3-diphenylaziridine in acetonitrile yields exclusively cis-3,5-diphenyl-1,2,4-dioxazolidine.Photooxygenation of N-alkyl-substituted 2,3-diphenylaziridines provides both isomers of the peroxide.The cis/tr

FORMATION OF A 1,2,4-DIOXAZOLIDINE BY ELECTRON-TRANSFER PHOTOOXYGENATION OF 1-BUTYL-2,3-DIPHENYLAZIRIDINE

Electron-transfer photooxygenation of 1-butyl-2,3-diphenylaziridine with 9,10-dicyanoanthracene in oxygen-saturated acetonitrile yields 4-butyl-3,5-diphenyl-1,2,4-dioxazolidine.This peroxide is surprisingly stable in nonpolar solvents decomposing to benzaldehyde and N-butylbenzamide upon heating to 100 deg C in benzene.Treatment with triphenyl phosphine yields benzaldehyde and N-butyl-1-phenylmethanimine.