3-(2-Chlorophenyl)-5-((4-chlorophenyl)methylene)-2-thioxo-4-imidazolidinone

Base Information

• Chemical Name: 3-(2-Chlorophenyl)-5-((4-chlorophenyl)methylene)-2-thioxo-4-imidazolidinone
• CAS No.: 74611-16-8
• Molecular Formula: C₁₆H₁₀Cl₂N₂OS
• Molecular Weight: 349.24
• Wikidata: Q76326803

Synonyms:BRN 0822535;3-o-Chlorofenylo-5-(p-chlorobenzylideno)-2-tiohydantoiny [Polish];3-(2-Chlorophenyl)-5-((4-chlorophenyl)methylene)-2-thioxo-4-imidazolidinone;4-IMIDAZOLIDINONE, 3-(2-CHLOROPHENYL)-5-((4-CHLOROPHENYL)METHYLENE)-2-THIOXO-;3-o-Chlorofenylo-5-(p-chlorobenzylideno)-2-tiohydantoiny;74611-16-8

Chemical Property of 3-(2-Chlorophenyl)-5-((4-chlorophenyl)methylene)-2-thioxo-4-imidazolidinone

Chemical Property:

• Vapor Pressure: 3.17E-09mmHg at 25°C
• Boiling Point: 476°Cat760mmHg
• Flash Point: 241.7°C
• Density: 1.52g/cm³
• XLogP3: 4.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 347.9890895
• Heavy Atom Count: 22
• Complexity: 489

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)N2C(=O)C(=CC3=CC=C(C=C3)Cl)NC2=S)Cl
• Isomeric SMILES: C1=CC=C(C(=C1)N2C(=O)/C(=C/C3=CC=C(C=C3)Cl)/NC2=S)Cl

Technology Process of 3-(2-Chlorophenyl)-5-((4-chlorophenyl)methylene)-2-thioxo-4-imidazolidinone

There total 1 articles about 3-(2-Chlorophenyl)-5-((4-chlorophenyl)methylene)-2-thioxo-4-imidazolidinone 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:

→ 5-(4-chloro-benzylidene)-3-(2-chloro-phenyl)-2-thioxo-imidazolidin-4-one (74611-16-8)

Guidance literature:

3-o-Chlorphenyl-2-thio-hydantoin, p-Chlorbenzaldehyd, Eg., Acetanhydrid, wsf. Natriumacetat, Kochen, 3-5 h, S. 168;

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