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

Base Information

Chemical Name:Ethyl (1E)-N-(4-chlorobenzoyl)ethanimidothioate
CAS No.:83253-09-2
Molecular Formula:C11H12ClNOS
Molecular Weight:241.741
Hs Code.:
DSSTox Substance ID:DTXSID70510166

Synonyms:83253-09-2;Ethyl (1E)-N-(4-chlorobenzoyl)ethanimidothioate;DTXSID70510166

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

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:241.0328129
Heavy Atom Count:15
Complexity:247

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)Cl)C

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

There total 2 articles about Ethyl (1E)-N-(4-chlorobenzoyl)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: 97.0%

: 2905-48-8
N-thioacetyl-4-chlorobenzamide

: 75-03-6
ethyl iodide

: 83253-09-2
4-Chloro-N-[1-ethylsulfanyl-eth-(Z)-ylidene]-benzamide

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

Reference yield:

: 83253-28-5
4-Chloro-N-[1-dimethylamino-eth-(E)-ylidene]-benzamide

: 83253-09-2
4-Chloro-N-[1-ethylsulfanyl-eth-(Z)-ylidene]-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / H₂S / acetic acid / Ambient temperature

2: 97 percent / K₂CO₃ / acetonitrile / 60 °C

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