4-((4-Chlorophenyl)methylene)-5-oxo-2-thioxo-1-imidazolidineacetic acid

Base Information

Chemical Name:4-((4-Chlorophenyl)methylene)-5-oxo-2-thioxo-1-imidazolidineacetic acid
CAS No.:79851-74-4
Molecular Formula:C₁₂H₉ClN₂O₃S
Molecular Weight:296.734
Hs Code.:
Wikidata:Q76326976

Synonyms:BRN 5972344;4-((4-Chlorophenyl)methylene)-5-oxo-2-thioxo-1-imidazolidineacetic acid;1-IMIDAZOLIDINEACETIC ACID, 4-((4-CHLOROPHENYL)METHYLENE)-5-OXO-2-THIOXO-;79851-74-4

Suppliers and Price of 4-((4-Chlorophenyl)methylene)-5-oxo-2-thioxo-1-imidazolidineacetic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-((4-Chlorophenyl)methylene)-5-oxo-2-thioxo-1-imidazolidineacetic acid

Chemical Property:

Vapor Pressure:2.3E-10mmHg at 25°C
Boiling Point:488.7°C at 760 mmHg
Flash Point:249.4°C
Density:1.6g/cm³
XLogP3:2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:296.0022410
Heavy Atom Count:19
Complexity:444

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C=C2C(=O)N(C(=S)N2)CC(=O)O)Cl
Isomeric SMILES:C1=CC(=CC=C1/C=C\2/C(=O)N(C(=S)N2)CC(=O)O)Cl

Technology Process of 4-((4-Chlorophenyl)methylene)-5-oxo-2-thioxo-1-imidazolidineacetic acid

There total 1 articles about 4-((4-Chlorophenyl)methylene)-5-oxo-2-thioxo-1-imidazolidineacetic acid 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: 64.2%

: 119681-50-4
2-(5-oxo-2-thioxoimidazolidin-1-yl) acetic acid

: 104-88-1
4-chlorobenzaldehyde

: 79851-74-4
5-p-chlorobenzylidene-2-thiohydantoin-3-acetic acid

Guidance literature:: With sodium acetate; acetic anhydride; In acetic acid; Heating;

Reference yield:

: 79851-74-4
5-p-chlorobenzylidene-2-thiohydantoin-3-acetic acid

: 79851-75-5
5-p-chlorobenzylidene-2-selenohydantoin-3-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) KOH / 1.) EtOH, reflux, 2.) EtOH, reflux, 15 min

2: 42.8 percent / NaHSe / ethanol / 1 h / Heating

With potassium hydroxide; sodium hydrogen selenide; In ethanol;

Reference yield:

: 79851-74-4
5-p-chlorobenzylidene-2-thiohydantoin-3-acetic acid

: 79851-81-3
potassium 2-methylseleno-4-p-chlorophenylmethylene-5-oxo-1-imidazoline acetate

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) KOH / 1.) EtOH, reflux, 2.) EtOH, reflux, 15 min

2: 42.8 percent / NaHSe / ethanol / 1 h / Heating

3: 1.) KOH / 1.) EtOH, reflux, 2.) EtOH, reflux, 15 min

With potassium hydroxide; sodium hydrogen selenide; In ethanol;