4-Thiazolidinone, 3-ethyl-5-((3-ethyl-2-thiazolidinylidene)ethylidene)-2-thioxo-

Base Information

Chemical Name:4-Thiazolidinone, 3-ethyl-5-((3-ethyl-2-thiazolidinylidene)ethylidene)-2-thioxo-
CAS No.:10505-40-5
Molecular Formula:C12H16 N2 O S3
Molecular Weight:300.47
Hs Code.:
European Community (EC) Number:234-033-9
Nikkaji Number:J212.433E
Mol file:10505-40-5.mol

Synonyms:EINECS 234-033-9;10505-40-5;3-Ethyl-5-(2-(3-ethylthiazolidin-2-ylidene)ethylidene)rhodanine;3-ethyl-5-[2-(3-ethylthiazolidin-2-ylidene)ethylidene]rhodanine;C12-H16-N2-O-S3;4-Thiazolidinone, 3-ethyl-5-((3-ethyl-2-thiazolidinylidene)ethylidene)-2-thioxo-;4-Thiazolidinone, 3-ethyl-5-[(3-ethyl-2-thiazolidinylidene)ethylidene]-2-thioxo-;3-Ethyl-5-[2-(3-ethylthiazolidin-2-ylidene)ethylidene]-2-thioxothiazolidin-4-one

Suppliers and Price of 4-Thiazolidinone, 3-ethyl-5-((3-ethyl-2-thiazolidinylidene)ethylidene)-2-thioxo-

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 6 raw suppliers

Chemical Property of 4-Thiazolidinone, 3-ethyl-5-((3-ethyl-2-thiazolidinylidene)ethylidene)-2-thioxo-

Chemical Property:

Vapor Pressure:4.64E-06mmHg at 25°C
Boiling Point:382.7°Cat760mmHg
Flash Point:185.2°C
PSA：106.24000
Density:1.37g/cm³
LogP:2.53640
XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:300.04247666
Heavy Atom Count:18
Complexity:431

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN1CCSC1=CC=C2C(=O)N(C(=S)S2)CC
Isomeric SMILES:CCN\1CCS/C1=C\C=C/2\C(=O)N(C(=S)S2)CC

Technology Process of 4-Thiazolidinone, 3-ethyl-5-((3-ethyl-2-thiazolidinylidene)ethylidene)-2-thioxo-

There total 5 articles about 4-Thiazolidinone, 3-ethyl-5-((3-ethyl-2-thiazolidinylidene)ethylidene)-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:

: 7648-01-3
3-ethylrhodanin

: 10505-40-5
3-ethyl-5-[2-(3-ethyl-thiazolidin-2-ylidene)-ethylidene]-2-thioxo-thiazolidin-4-one

Guidance literature:: Multi-step reaction with 3 steps

1: petroleum ether / 120 °C

2: acetic acid anhydride; triethylamine

3: triethylamine; ethanol

With ethanol; acetic anhydride; triethylamine; Petroleum ether;
DOI:10.1021/ja01155a095

Reference yield:

: 3747-06-6
N-(3-ethyl-4-oxo-2-thioxothiazolidin-5-ylidenemethyl)-N-phenylacetamide

: 54654-71-6
2-methyl-3-ethyl-4,5-dihydrothiazolium iodide

: 10505-40-5
3-ethyl-5-[2-(3-ethyl-thiazolidin-2-ylidene)-ethylidene]-2-thioxo-thiazolidin-4-one

Guidance literature:: With ethanol; triethylamine;
DOI:10.1021/ja01155a095

Reference yield:

: 39542-83-1
3-ethyl-5-((phenylamino)methylene)-2-thioxothiazolidin-4-one

: 10505-40-5
3-ethyl-5-[2-(3-ethyl-thiazolidin-2-ylidene)-ethylidene]-2-thioxo-thiazolidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid anhydride; triethylamine

2: triethylamine; ethanol

With ethanol; acetic anhydride; triethylamine;
DOI:10.1021/ja01155a095