1-PHENYLIMIDAZOLIDINE-2,4,5-TRIONE

Base Information

• Chemical Name: 1-PHENYLIMIDAZOLIDINE-2,4,5-TRIONE
• CAS No.: 2211-33-8
• Molecular Formula: C9H6 N2 O3
• Molecular Weight: 190.158
• Hs Code.: 2933990090
• Mol file: 2211-33-8.mol

Synonyms:Imidazolidinetrione,phenyl- (7CI,9CI); Parabanic acid, 1-phenyl- (6CI);1-Phenyl-3,4,5-trioxoimidazolidine; 1-Phenylimidazolidine-2,4,5-trione;Phenylparabanic acid

Chemical Property of 1-PHENYLIMIDAZOLIDINE-2,4,5-TRIONE

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 66.48000
• Density: 1.468g/cm³
• LogP: 0.66320

Purity/Quality:

99% ^*data from raw suppliers

1-phenylimidazolidine-2,4,5-trione ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of 1-PHENYLIMIDAZOLIDINE-2,4,5-TRIONE

There total 10 articles about 1-PHENYLIMIDAZOLIDINE-2,4,5-TRIONE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

oxalyl dichloride (79-37-8) + phenyl carbamate (64-10-8) → N-phenylparabanic acid (2211-33-8)

Guidance literature:

In benzene; at 20 ℃;

Reference yield: 56.0%

ethyl 2-ethoxy-2-iminoacetate (816-27-3) + phenyl carbamate (64-10-8) → N-phenylparabanic acid (2211-33-8)

Guidance literature:

With hydrogenchloride; In tetrahydrofuran; Heating;

DOI:10.1016/S0040-4020(01)90547-2

Reference yield: 30.0%

N-(5,5-diethoxy-2-oxo-3-phenylimidazolidin-4-ylidene)-N'-phenylurea (88039-12-7) → N-phenylparabanic acid (2211-33-8) + phenyl carbamate (64-10-8)

Guidance literature:

With hydrogenchloride; for 0.333333h; Heating;

upstream raw materials:

phenyl carbamate

Ethyl oxalyl chloride

oxalic acid diethyl ester

oxalyl dichloride

Downstream raw materials:

2-(dimethylamino)-7a-hydroxy-3,3-dimethyl-6-phenyl-5,6,7,7a-tetrahydro-3H-imidazo<3,4-a>imidazol-5,7-dion

1-phenyl-3-(1,1,3-trioxo-2,3-dihydro-1λ⁶-benzo[d]isothiazol-2-ylmethyl)imidazolidine-2,4,5-trione

phenyl carbamate

1-(benzimidazol-1-ylmethyl)-3-phenyl-imidazolidine-2,4,5-trione

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