498534-36-4

Upstream product

• 6630-33-7 ortho-bromobenzaldehyde 
• 53606-33-0 2-(ethylsulfanyl)benzenecarbaldehyde 
• 37527-69-8 (2-ethylsulfanyl-phenyl)-methanol 

Downstream Products

• 873193-39-6 3-(o-ethylthiobenzyl)-4-hydroxy-5,5-dimethylimidazolidin-2-one 
• 873193-41-0 1-(o-ethylthiobenzyl)-4,5-dimethylimidazol-2(3H)-one 
• 873193-37-4 3-(o-ethylthiobenzyl)-5,5-dimethylhydantoin 
• 498534-34-2 2-(2'-ethylsulfonylbenzyl)-1,10-phenanthroline 
• 498534-32-0 2-(2'-ethylthiobenzyl)-1,10-phenanthroline 

Relevant academic research and scientific papers

Three-Dimensional Heterocycles by Iron-Catalyzed Ring-Closing Sulfoxide Imidation

A general and atom-economical method for the synthesis of cyclic sulfoximines by intramolecular imidations of azido-containing sulfoxides using a commercially available FeII phthalocyanine (FeIIPc) as catalyst has been developed. The method conveys a broad functional group tolerance and the resulting three-dimensional heterocycles can be modified by cross-coupling reactions.

Synthesis of 2-benzyl-1,10-phenanthrolines substituted by sulfoxide or sulfone groups as potential photochromic compounds

New 2-benzyl-1,10-phenanthrolines, substituted at the 2′ position by electron-withdrawing groups, were synthesized through nucleophilic substitution involving 2-chloro-1,10-phenanthroline and substituted benzyllithiums, respectively. The expected reversible photoinduced proton transfer reaction of such compounds were studied.