2211-33-8

Basic information

• Product Name: 1-PHENYLIMIDAZOLIDINE-2,4,5-TRIONE
• Synonyms: Imidazolidinetrione,phenyl- (7CI,9CI); Parabanic acid, 1-phenyl- (6CI);1-Phenyl-3,4,5-trioxoimidazolidine; 1-Phenylimidazolidine-2,4,5-trione;Phenylparabanic acid
• CAS NO: 2211-33-8
• Molecular Formula: C₉H₆N₂O₃
• Molecular Weight: 0
• Mol File: 2211-33-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.468g/cm³
• Refractive Index: 1.621
• CAS DataBase Reference: 1-PHENYLIMIDAZOLIDINE-2,4,5-TRIONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-PHENYLIMIDAZOLIDINE-2,4,5-TRIONE(2211-33-8)
• EPA Substance Registry System: 1-PHENYLIMIDAZOLIDINE-2,4,5-TRIONE(2211-33-8)

Safety Data

• Hazardous Substances Data: 2211-33-8(Hazardous Substances Data)

Usage

Uses

1-Phenylimidazolidine-2,4,5-trione can be used as anticancer agents.

InChI:InChI=1/C9H6N2O3/c12-7-8(13)11(9(14)10-7)6-4-2-1-3-5-6/h1-5H,(H,10,12,14)

Upstream product

• 64-10-8 phenyl carbamate 
• 4755-77-5 Ethyl oxalyl chloride 
• 816-27-3 ethyl 2-ethoxy-2-iminoacetate 
• 88039-11-6 1-(4-ethoxy-2-oxo-1-phenyl-3-imidazolin-5-ylidene)-3-phenylurea 
• 79-37-8 oxalyl dichloride 
• 2010-15-3 3-phenyl-2-thioxoimidazolidin-4-one 
• 88039-12-7 N-(5,5-diethoxy-2-oxo-3-phenylimidazolidin-4-ylidene)-N'-phenylurea 
• 95-92-1 oxalic acid diethyl ester 

Downstream Products

• 170379-67-6 N-chloromethyl-N'-phenyl-2,4,5-imidazolidinetrione 
• 41300-33-8 2,4,5-trioxo-3-phenyl-imidazolidine-1-carboxylic acid methylamide 
• 1086764-80-8 C₁₂H₁₀N₂O₅ 
• 65081-79-0 2-(N'-phenyl-ureido)-butyric acid 
• 1207374-48-8 1-[(3-phenylimidazolidine-2,4,5-trionyl)methyl]-3-methyl-imidazolidine-2,4,5-trione 
• 1207374-50-2 1-ethyl-3-((2,4,5-trioxo-3-phenylimidazolidin-1-yl)methyl)imidazolidine-2,4,5-trione 
• 246858-22-0 1-phenyl-3-(1,1,3-trioxo-2,3-dihydro-1λ⁶-benzo[d]isothiazol-2-ylmethyl)imidazolidine-2,4,5-trione 
• 64-10-8 phenyl carbamate 
• 1421005-13-1 1-(benzimidazol-1-ylmethyl)-3-phenyl-imidazolidine-2,4,5-trione 
• 153782-12-8 2-(dimethylamino)-7a-hydroxy-3,3-dimethyl-6-phenyl-5,6,7,7a-tetrahydro-3H-imidazo<3,4-a>imidazol-5,7-dion 

Relevant articles and documents

Simple synthesis of imidazolidinetrione derivatives having imidazolidine-2,4,5-trione and 2-thioxo-imidazolidine-4,5-dione rings

As a part of a research program related to the synthetic study of pharmacologically and agrochemically important imidazolidines, we chose to identify imidazolidine-2,4,5-trione and imidazolidine-2,4,5-trione or 2-thioxo-imidazolidine-4,5-dione rings as active components for the desired property. We currently report the synthesis of (imidazolidin.-2,4,5-dionyl) methyl-imidazolidine-2,4,5-triones 1, 4,5-dioxo-2-thioxo-imidazolidin-1.-yl- methyl-imidazolidine-2,4,5-triones 2, and 4,5-dioxo-2-thioxo-imidazolidin-1- ylmethyl-imidazolidine-2-thioxo-4,5-dione 3.

Ring-Transformationen bei der Umsetzung von 3-(Dimethylamino)-2,2-dimethyl-2H-azirin mit 1-substituierten Imidazolidin-2,4,5-trionen

Reaction of 1-substituted imidazolidine-2,4,5-triones ( = N-substituted parabanic acids; 2) and 3-(dimethylamino)-2,2-dimethyl-2H-azirine (1) in i-PrOH or MeCN at room temperature yields 5,6,7,7a-tetrahydro-3H-imidazoimidazole-5,7-diones 3 (Scheme

The Structure of the Phenyl Isocyanate - Ethyl 1-Cyanoformimidate Adducts.

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