4-Imidazolidinone, 3-ethyl-1-phenyl-2-thioxo-

Base Information

• Chemical Name: 4-Imidazolidinone, 3-ethyl-1-phenyl-2-thioxo-
• CAS No.: 37021-14-0
• Molecular Formula: C11H12 N2 O S
• Molecular Weight: 220.295
• Hs Code.: 2933990090
• European Community (EC) Number: 253-310-5
• DSSTox Substance ID: DTXSID6068018
• Nikkaji Number: J260.719K
• Wikidata: Q81994711
• Mol file: 37021-14-0.mol

Synonyms:3-Ethyl-1-phenyl-2-thioxoimidazolidin-4-one;37021-14-0;4-Imidazolidinone, 3-ethyl-1-phenyl-2-thioxo-;3-ethyl-1-phenyl-2-sulfanylideneimidazolidin-4-one;EINECS 253-310-5;3-Ethyl-1-phenyl-2-thioxo-4-imidazolidinone;DTXSID6068018;SCHEMBL10383197;3-Ethyl-1-phenyl-2-thiohydantoin;HMS1577P01;MFCD00541210;STK075482;AKOS000313236;3-Ethyl-1-phenyl-2-thiohydantoin, 95%;CS-0298309;EN300-230543;3-Ethyl-1-phenyl-2-thioxo-4-imidazolidinone #;SR-01000389512;SR-01000389512-1;3-ethyl-1-phenyl-2-thioxotetrahydro-4H-imidazol-4-one;5107-57-3

Chemical Property of 4-Imidazolidinone, 3-ethyl-1-phenyl-2-thioxo-

Chemical Property:

• Vapor Pressure: 0.000591mmHg at 25°C
• Boiling Point: 310.7°Cat760mmHg
• Flash Point: 141.7°C
• PSA: 55.64000
• Density: 1.3g/cm³
• LogP: 1.64290
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 220.06703418
• Heavy Atom Count: 15
• Complexity: 274

Purity/Quality:

99% ^*data from raw suppliers

3-ETHYL-1-PHENYL-2-THIOXO-1,3-DIAZOLIDIN-4-ONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN1C(=O)CN(C1=S)C2=CC=CC=C2

Technology Process of 4-Imidazolidinone, 3-ethyl-1-phenyl-2-thioxo-

There total 1 articles about 4-Imidazolidinone, 3-ethyl-1-phenyl-2-thioxo- 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: 54.0%

N-phenylglycine ethyl ester (2216-92-4) + Ethyl isothiocyanate (542-85-8) → 3-ethyl-1-phenyl-2-thioxo-imidazolidin-4-one (37021-14-0)

Guidance literature:

Reference yield: 66.0%

3-ethyl-1-phenyl-2-thioxo-imidazolidin-4-one (37021-14-0) + 3-Formylchromone (17422-74-1) → 2-thioxo-5-[(4-oxo-4H-[1]benzopyran-3-yl)methylidene]-N1-phenyl-N3-ethyl-imidazolidin-4-one

Guidance literature:

With sodium acetate; acetic acid; Heating;

DOI:10.1080/10426500490494769

Reference yield:

diethoxymethyl acetate (14036-06-7) + 3-ethyl-1-phenyl-2-thioxo-imidazolidin-4-one (37021-14-0) → 3,3'-diethyl-1,1'-diphenyl-2,2'-dithioxo-5,5'-methanylylidene-bis-imidazolidin-4-one

Guidance literature:

With piperidine; at 120 ℃;

DOI:10.1021/ja01155a095

upstream raw materials:

N-phenylglycine ethyl ester

Ethyl isothiocyanate

Downstream raw materials:

3-ethyl-5-(1-ethyl-1H-[4]pyridylidene)-1-phenyl-2-thioxo-imidazolidin-4-one

5-cyclopentylidene-3-ethyl-1-phenyl-2-thioxo-imidazolidin-4-one