1426307-47-2

Upstream product

• 99-91-2 para-chloroacetophenone 
• 106-47-8 4-chloro-aniline 
• 536-38-9 4-chlorobenzoylmethyl bromide 

Downstream Products

• 1446221-45-9 2,4,6-tri(4-chlorophenyl)-4H-1,4-oxazine 
• 36004-83-8 (4-chlorophenyl)(3-phenyl-1H-2-indolyl)methanone 
• 106-47-8 4-chloro-aniline 
• 1426307-56-3 [5-chloro-3-(2-fluorophenyl)-1H-2-indolyl](4-chlorophenyl)methanone 
• 37600-82-1 (4-chlorophenyl)(5-chloro-3-phenyl-1H-2-indolyl)methanone 

Relevant academic research and scientific papers

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.

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 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