52230-56-5

Upstream product

• 502-49-8 cycloactanone 
• 89-98-5 2-chloro-benzaldehyde 

Downstream Products

• 52186-10-4 2,8-Bis-(2-chlor-benzyl)-cyclooctanon 
• 77109-61-6 4-(2-Chloro-phenyl)-10-[1-(2-chloro-phenyl)-meth-(E)-ylidene]-3,4,5,6,7,8,9,10-octahydro-1H-cyclooctapyrimidine-2-thione 
• 77109-74-1 4-(2-Chloro-phenyl)-2-[1-(2-chloro-phenyl)-meth-(Z)-ylidene]-10-[1-(2-chloro-phenyl)-meth-(E)-ylidene]-5,6,7,8,9,10-hexahydro-4H-1-thia-3a,11-diaza-cycloocta[f]inden-3-one 
• 77109-78-5 5-(2-Chloro-phenyl)-11-[1-(2-chloro-phenyl)-meth-(E)-ylidene]-2,3,6,7,8,9,10,11-octahydro-5H-1-thia-4a,12-diaza-cycloocta[b]naphthalen-4-one 
• 77109-67-2 4-(2-Chloro-phenyl)-10-[1-(2-chloro-phenyl)-meth-(E)-ylidene]-5,6,7,8,9,10-hexahydro-4H-1-thia-3a,11-diaza-cycloocta[f]inden-3-one 

Relevant academic research and scientific papers

Reactions with (Arylmethylene)cycloalkanones. 3. Synthesis of 11-(Arylmethylene)octahydrocyclooctathiazolopyrimidin-3-one Derivatives of Expected Biological Activity

Cyclooctapyrimidine-2-thiones (II) were prepared by heating 2,8-bis(arylmethylene)cyclooctanones with thiourea in ethanolic potassium hydroxide.Compounds II reacted with chloroacetic acid to yield the title compounds (III).The 2,11-bis(arylmethylene) d