Ethyl (1E)-N-(4-methoxybenzoyl)ethanimidothioate

Base Information

Chemical Name:Ethyl (1E)-N-(4-methoxybenzoyl)ethanimidothioate
CAS No.:83253-07-0
Molecular Formula:C12H15NO2S
Molecular Weight:237.323
Hs Code.:
DSSTox Substance ID:DTXSID10510165

Synonyms:83253-07-0;Ethyl (1E)-N-(4-methoxybenzoyl)ethanimidothioate;DTXSID10510165

Suppliers and Price of Ethyl (1E)-N-(4-methoxybenzoyl)ethanimidothioate

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 1 raw suppliers

Chemical Property of Ethyl (1E)-N-(4-methoxybenzoyl)ethanimidothioate

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:237.08234989
Heavy Atom Count:16
Complexity:258

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCSC(=NC(=O)C1=CC=C(C=C1)OC)C

Technology Process of Ethyl (1E)-N-(4-methoxybenzoyl)ethanimidothioate

There total 2 articles about Ethyl (1E)-N-(4-methoxybenzoyl)ethanimidothioate 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: 91.0%

: 83253-13-8
N-Thioacetyl-p-anisamide

: 75-03-6
ethyl iodide

: 83253-07-0
Ethyl N-p-Anisolylthioactimidate

Guidance literature:: With potassium carbonate; In acetonitrile; at 60 ℃; for 2.5h;

Reference yield:

: 83253-27-4
N-<(Dimethylamino)ethylidene>-p-anisamide

: 83253-07-0
Ethyl N-p-Anisolylthioactimidate

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / H₂S / acetic acid / 0.17 h / Ambient temperature

2: 91 percent / K₂CO₃ / acetonitrile / 2.5 h / 60 °C

With hydrogen sulfide; potassium carbonate; In acetic acid; acetonitrile;