932022-91-8

Upstream product

• 62-53-3 aniline 
• 536-38-9 4-chlorobenzoylmethyl bromide 
• 99-91-2 para-chloroacetophenone 

Downstream Products

• 1026148-83-3 4,10a-bis(4-chlorophenyl)-2-phenyl-1,10a-dihydro-2H-pyrazino[2,1-b][1,3]benzoxazole 
• 1446221-21-1 2,6-bis(4-chlorophenyl)-4-phenyl-4H-1,4-oxazine 
• 1426307-56-3 [5-chloro-3-(2-fluorophenyl)-1H-2-indolyl](4-chlorophenyl)methanone 
• 62-53-3 aniline 
• 17286-63-4 2-(4-chlorophenyl)quinoxaline 
• 1172627-51-8 3-(4-chlorophenyl)-1-(1-phenylethyl)-1,4-dihydroquinoxaline 

Relevant academic research and scientific papers

Ultrasound-mediated synthesis of N,N-bis(phenacyl)aniline under solvent-free conditions

An efficient method for the synthesis of N,N-bis(phenacyl)anilines was developed via smooth condensation of anilines with α-bromoacetophenones in the presence of sodium carbonate as acid acceptor and polyethylene glycol 400 (PEG 400) as catalyst at room t

Synthesis and photochemical properties of 2,4,6,-triaryl-4h-1,4-oxazines

A series of 2,4,6-triaryl-4H-1,4-oxazines was synthesized, and their photochemical properties were studied. The 2,4,6-triaryl-4H-1,4-oxazines underwent photoreaction to N-(1-methoxy-2-oxo-2-arylethyl)-N-arylformamides determined by 1H NMR, 13C NMR, MS, and single crystal X-ray diffraction analyses.

Synthesis of 4H-1,4-oxazines as transthyretin amyloid fibril inhibitors

4H-1,4-oxazines were designed as transthyretin (TTR) amyloid fibril inhibitors based on an analysis of the interactions between known small molecule inhibitors and TTR by molecular docking. A series of 2,4,6-triaryl-4H-1,4- oxazines was synthesized by the

Synthesis of novel 3,5,7-triaryl-5,6-dihydro-4H-1,2,5-triazepines

(Chemical Equation Presented) Several hitherto unknown 3,5,7-triaryl-5,6- dihydro-4H-1,2,5-triazepines have been synthesised by cyclocondensation of N,N-bis(phenacyl)anilines with hydrazine hydrate in ethanol or ethyleneglycol under reflux condition. Incr