(5E)-5-benzylidene-3-phenyl-1,3-thiazolidine-2,4-dione

Base Information

Chemical Name:(5E)-5-benzylidene-3-phenyl-1,3-thiazolidine-2,4-dione
CAS No.:42518-27-4
Molecular Formula:C16H11NO2S
Molecular Weight:281.335
Hs Code.:
NSC Number:153114
Mol file:42518-27-4.mol

Synonyms:42518-27-4;NSC153114;(5E)-5-benzylidene-3-phenyl-1,3-thiazolidine-2,4-dione;SCHEMBL9911664;HMS1680H04;AKOS000631232;NSC-153114;A826121;SR-01000369251;SR-01000369251-1;(5E)-3-phenyl-5-(phenylmethylene)thiazolidine-2,4-dione;(5E)-3-phenyl-5-(phenylmethylidene)-1,3-thiazolidine-2,4-dione

Suppliers and Price of (5E)-5-benzylidene-3-phenyl-1,3-thiazolidine-2,4-dione

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of (5E)-5-benzylidene-3-phenyl-1,3-thiazolidine-2,4-dione

Chemical Property:

Vapor Pressure:6.35E-08mmHg at 25°C
Boiling Point:439.5°Cat760mmHg
Flash Point:219.6°C
Density:1.377g/cm³
XLogP3:3.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:281.05104977
Heavy Atom Count:20
Complexity:420

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C=C2C(=O)N(C(=O)S2)C3=CC=CC=C3
Isomeric SMILES:C1=CC=C(C=C1)/C=C/2\C(=O)N(C(=O)S2)C3=CC=CC=C3

Technology Process of (5E)-5-benzylidene-3-phenyl-1,3-thiazolidine-2,4-dione

There total 9 articles about (5E)-5-benzylidene-3-phenyl-1,3-thiazolidine-2,4-dione 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: 83.0%

: 3774-99-0
5-benzylidene-2,4-thiazolidinedione

: diphenyliodonium tetrafluoroborate

: 42518-27-4
5-Benzyliden-3-phenylthiazolidin-2,4-dion

Guidance literature:: With potassium hydroxide; 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate; at 80 ℃; for 2h;
DOI:10.3184/030823408X382144

Reference yield: 32.0%

: 138696-25-0
5-Benzyliden-3-phenyl-4-oxothiazolidin-2-thion-S-oxid

: 42518-27-4
5-Benzyliden-3-phenylthiazolidin-2,4-dion

Guidance literature:: With potassium peroxomonosulfate; ethylenediaminetetraacetic acid; 3,3-dimethyldioxirane; In dichloromethane; water; acetone; Ambient temperature; 1 M KH₂PO₄/Na₂HPO₄-buffer;