66502-22-5

Upstream product

• 151-50-8 potassium cyanide 
• 66502-26-9 2-morpholino-1-phenyl-ethanone; hydrochloride 

Downstream Products

• 66502-08-7 1,3-bis-benzenesulfonyl-5-morpholin-4-ylmethyl-5-phenyl-imidazolidine-2,4-dione 
• 66502-10-1 3,5-bis-morpholin-4-ylmethyl-5-phenyl-imidazolidine-2,4-dione 
• 7507-24-6 5-hydroxymethyl-5-phenyl-imidazolidine-2,4-dione 

Relevant academic research and scientific papers

Racemates and enantiomers of basic substituted 5-phenylhydantoins. Syntheses and antiarrhythmic activity

The racemates and the enantiomers of 5-phenylhydantoins with basic substituents in 5-position are synthesized on two different routes via the Bucherer-Bergs-reaction. Using lanthanide-shift-reagents the enantiomeric excess for the enantiomers of 3-methyl-

Hydantoin derivatives as potential antiinflammatory agents

The hydantoins 2a-c and three hydantoic acids were synthesized and their anti-inflammatory properties were determined in the rat paw oedema test. Neither 1-phenyl-sulphonyl-5,5-diphenylhydantoin, which has been described as an inflammatory, nor any of the other compounds, showed significant anti-inflammatory activity.