3,5,5-Triphenyl-2-thioxo-4-imidazolidinone

Base Information

Chemical Name:3,5,5-Triphenyl-2-thioxo-4-imidazolidinone
CAS No.:52460-98-7
Molecular Formula:C21H16N2OS
Molecular Weight:344.437
Hs Code.:
DSSTox Substance ID:DTXSID40418842
Nikkaji Number:J615.901J
ChEMBL ID:CHEMBL353091
Mol file:52460-98-7.mol

Synonyms:52460-98-7;3,5,5-Triphenyl-2-thioxo-4-imidazolidinone;3,5,5-triphenyl-2-sulfanylideneimidazolidin-4-one;3,5,5-triphenyl-2-thioxoimidazolidin-4-one;thiohydantoin compound, 2;4-Imidazolidinone, 3,5,5-triphenyl-2-thioxo-;CHEMBL353091;BDBM23311;DTXSID40418842;VYCBHDCXQUZIJV-UHFFFAOYSA-N

Suppliers and Price of 3,5,5-Triphenyl-2-thioxo-4-imidazolidinone

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of 3,5,5-Triphenyl-2-thioxo-4-imidazolidinone

Chemical Property:

XLogP3:4.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:344.09833431
Heavy Atom Count:25
Complexity:484

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2(C(=O)N(C(=S)N2)C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of 3,5,5-Triphenyl-2-thioxo-4-imidazolidinone

There total 5 articles about 3,5,5-Triphenyl-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: 93.0%

: 134-81-6
benzil

: 103-85-5
monophenylthiourea

: 52460-98-7
3,5,5-triphenyl-2-thioxo-imidazolidin-4-one

Guidance literature:: With potassium hydroxide; for 3h; Heating;
DOI:10.1021/jm00155a042

Reference yield:

: 741-36-6
1,1-diphenyl-1-chloroacetanilide

: 1147550-11-5
ammonium thiocyanate

: 52460-98-7
3,5,5-triphenyl-2-thioxo-imidazolidin-4-one

Guidance literature:: With acetone;
DOI:10.1021/ja01303a050

Reference yield:

: 100-52-7
benzaldehyde

: 52460-98-7
3,5,5-triphenyl-2-thioxo-imidazolidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: Thiamine hydrochloride / 0.5 h / Reflux; Green chemistry

2: hydrogenchloride / Green chemistry

With hydrogenchloride; Thiamine hydrochloride;
DOI:10.1002/jhet.3308