2-(1-(2-(4-trifluoromethylphenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarbothioamide

Base Information

Chemical Name:2-(1-(2-(4-trifluoromethylphenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarbothioamide
CAS No.:1383485-09-3
Molecular Formula:C₁₇H₁₄F₃N₅S
Molecular Weight:377.393
Hs Code.:

Synonyms:2-(1-(2-(4-trifluoromethylphenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarbothioamide

Suppliers and Price of 2-(1-(2-(4-trifluoromethylphenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarbothioamide

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

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Chemical Property of 2-(1-(2-(4-trifluoromethylphenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarbothioamide

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Technology Process of 2-(1-(2-(4-trifluoromethylphenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarbothioamide

There total 4 articles about 2-(1-(2-(4-trifluoromethylphenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarbothioamide 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: 64.0%

: 1383484-93-2
2-(4-trifluoromethylphenyl)-5-acetyl-1H-benzimidazole

: 79-19-6
thiosemicarbazide

: 1383485-09-3
2-(1-(2-(4-trifluoromethylphenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarbothioamide

Guidance literature:: With acetic acid; In ethanol; water; for 1h; Reflux;
DOI:10.1016/j.ejmech.2012.03.038

Reference yield:

: 152782-75-7
sodium hydroxy(4-(trifluoromethyl)phenyl)methanesulfonate

: 1383485-09-3
2-(1-(2-(4-trifluoromethylphenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol / 4 h / Reflux

2: acetic acid / ethanol; water / 1 h / Reflux

With acetic acid; In ethanol; water;
DOI:10.1016/j.ejmech.2012.03.038

Reference yield:

: 455-19-6
4-Trifluoromethylbenzaldehyde

: 1383485-09-3
2-(1-(2-(4-trifluoromethylphenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarbothioamide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium disulfite / ethanol

2: ethanol / 4 h / Reflux

3: acetic acid / ethanol; water / 1 h / Reflux

With sodium disulfite; acetic acid; In ethanol; water;
DOI:10.1016/j.ejmech.2012.03.038