2-[1-(5-chloro-1H-benzimidazol-2-yl)ethylidene]-N-cyclohexylhydrazine carbothioamide

Base Information

Chemical Name:2-[1-(5-chloro-1H-benzimidazol-2-yl)ethylidene]-N-cyclohexylhydrazine carbothioamide
CAS No.:1426544-51-5
Molecular Formula:C₁₆H₂₀ClN₅S
Molecular Weight:349.887
Hs Code.:

Synonyms:

Suppliers and Price of 2-[1-(5-chloro-1H-benzimidazol-2-yl)ethylidene]-N-cyclohexylhydrazine carbothioamide

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 0 raw suppliers

Chemical Property of 2-[1-(5-chloro-1H-benzimidazol-2-yl)ethylidene]-N-cyclohexylhydrazine carbothioamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-[1-(5-chloro-1H-benzimidazol-2-yl)ethylidene]-N-cyclohexylhydrazine carbothioamide

There total 3 articles about 2-[1-(5-chloro-1H-benzimidazol-2-yl)ethylidene]-N-cyclohexylhydrazine 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: 70.0%

: 21198-18-5
4-cyclohexyl-thiosemicarbazide

: 41510-16-1
1-(5-chloro-1H-benzo[d]imidazol-2-yl)-1-ethanone

: 1426544-51-5
2-[1-(5-chloro-1H-benzimidazol-2-yl)ethylidene]-N-cyclohexylhydrazine carbothioamide

Guidance literature:: With acetic acid; In methanol; for 2h; Reflux;

Reference yield:

: 95-83-0
4-Chloro-1,2-phenylenediamine

: 1426544-51-5
2-[1-(5-chloro-1H-benzimidazol-2-yl)ethylidene]-N-cyclohexylhydrazine carbothioamide

Guidance literature:: Multi-step reaction with 3 steps

1: 0.58 h / Microwave irradiation

2: acetic acid; chromium(VI) oxide / water / 87 - 92 °C

3: acetic acid / methanol / 2 h / Reflux

With chromium(VI) oxide; acetic acid; In methanol; water;

Reference yield:

: 20033-96-9
1-(5-chloro-1H-benzo[d]imidazo l-2-yl)ethan-1-ol

: 1426544-51-5
2-[1-(5-chloro-1H-benzimidazol-2-yl)ethylidene]-N-cyclohexylhydrazine carbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid; chromium(VI) oxide / water / 87 - 92 °C

2: acetic acid / methanol / 2 h / Reflux

With chromium(VI) oxide; acetic acid; In methanol; water;