856-85-9

Basic information

• Product Name: 3-(morpholin-4-ylmethyl)-5,5-diphenylimidazolidine-2,4-dione
• Synonyms: 2,4-imidazolidinedione, 3-(4-morpholinylmethyl)-5,5-diphenyl-; 3-(Morpholin-4-ylmethyl)-5,5-diphenylimidazolidine-2,4-dione
• CAS NO: 856-85-9
• Molecular Formula: C₂₀H₂₁N₃O₃
• Molecular Weight: 351.399
• Mol File: 856-85-9.mol
• Article Data: 2

Chemical Properties

• Density: 1.264g/cm³
• Refractive Index: 1.608
• CAS DataBase Reference: 3-(morpholin-4-ylmethyl)-5,5-diphenylimidazolidine-2,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(morpholin-4-ylmethyl)-5,5-diphenylimidazolidine-2,4-dione(856-85-9)
• EPA Substance Registry System: 3-(morpholin-4-ylmethyl)-5,5-diphenylimidazolidine-2,4-dione(856-85-9)

Safety Data

• Hazardous Substances Data: 856-85-9(Hazardous Substances Data)

Upstream product

• 134-81-6 benzil 
• 110-91-8 morpholine 
• 50-00-0 formaldehyd 
• 57-41-0 phenythoin 

Downstream Products

• 6859-11-6 1-methyl-5,5-diphenylimidazolidine-2,4-dione 
• 86254-11-7 5-hydroxy-3,3-diphenyl-11-oxa-4,6,8-triazatricyclo<6.4.0.0^2,6>dodecan-5-one 

Relevant articles and documents

Microwave-assisted synthesis of some novel and potent antibacterial and antifungal compounds with biological screening

Hydantoins have widely been used as antiarrythmic, anticonvulsant and antitumor agents but recent research has shown a different and novel cytotoxic activity of hydantoins and its derivatives, i.e. anti HIV, antibacterial and antifungal. The following research article deals with the synthesis of hydantoins and their derivatives by Mannich reaction viz., 3-(substituted)-5,5- diphenylimidazolidine-2,4-dione and 1-(substituted)-3,5,5- triphenylimidazolidine-2,4-dione. The synthesised compounds are novel and some of the compounds showed good antibacterial and antifungal activity equivalent to the standards used. All synthetic procedures were carried out in a microwave and not by conventional methods, which led to speedy process and high yield for the same. Springer Science+Business Media, LLC 2011.