(E)-2-(4-chlorophenylimino)-N-(4-chlorophenyl)imidazolidine-1-carbothioamide

Base Information

Chemical Name:(E)-2-(4-chlorophenylimino)-N-(4-chlorophenyl)imidazolidine-1-carbothioamide
CAS No.:883104-32-3
Molecular Formula:C₁₆H₁₄Cl₂N₄S
Molecular Weight:365.286
Hs Code.:

Synonyms:(E)-2-(4-chlorophenylimino)-N-(4-chlorophenyl)imidazolidine-1-carbothioamide

Suppliers and Price of (E)-2-(4-chlorophenylimino)-N-(4-chlorophenyl)imidazolidine-1-carbothioamide

Supply Marketing:

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

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Chemical Property of (E)-2-(4-chlorophenylimino)-N-(4-chlorophenyl)imidazolidine-1-carbothioamide

Chemical Property:

Purity/Quality:

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Technology Process of (E)-2-(4-chlorophenylimino)-N-(4-chlorophenyl)imidazolidine-1-carbothioamide

There total 2 articles about (E)-2-(4-chlorophenylimino)-N-(4-chlorophenyl)imidazolidine-1-carbothioamide 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:

: 97754-55-7
C₁₆H₁₆Cl₂N₄S₂

: 883104-32-3
(E)-2-(4-chlorophenylimino)-N-(4-chlorophenyl)imidazolidine-1-carbothioamide

Guidance literature:: With copper(II) choride dihydrate; sodium carbonate; In ethanol; at 25 ℃; for 10h;
DOI:10.1002/ejoc.201501096

Reference yield:

: 2131-55-7
4-Chlorophenyl isothiocyanate

: 883104-32-3
(E)-2-(4-chlorophenylimino)-N-(4-chlorophenyl)imidazolidine-1-carbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: copper(II) choride dihydrate / ethanol / 0.33 h / 25 °C

2: copper(II) choride dihydrate; sodium carbonate / ethanol / 10 h / 25 °C

With copper(II) choride dihydrate; sodium carbonate; In ethanol;
DOI:10.1002/ejoc.201501096