benzyl benzimidothioate

Base Information

Chemical Name:benzyl benzimidothioate
CAS No.:72875-44-6
Molecular Formula:C₁₄H₁₃NS
Molecular Weight:227.33
Hs Code.:

Synonyms:benzyl benzimidothioate

Suppliers and Price of benzyl benzimidothioate

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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 benzyl benzimidothioate

Chemical Property:

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Technology Process of benzyl benzimidothioate

There total 5 articles about benzyl benzimidothioate 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: 55.0%

: 100-39-0
benzyl bromide

: 2227-79-4
benzenecarbothioamide

: 72875-44-6
benzyl benzimidothioate

Guidance literature:: In chloroform; for 12h; Reflux;
DOI:10.1021/acs.jmedchem.7b00888

Reference yield:

: 98-88-4
benzoyl chloride

: 72875-44-6
benzyl benzimidothioate

Guidance literature:: Multi-step reaction with 3 steps

1: ammonium hydroxide; triethylamine / toluene / 24 h / 20 °C

2: Lawessons reagent / tetrahydrofuran / 12 h / 20 °C

3: chloroform / 12 h / Reflux

With Lawessons reagent; ammonium hydroxide; triethylamine; In tetrahydrofuran; chloroform; toluene;
DOI:10.1021/acs.jmedchem.7b00888

Reference yield:

: 55-21-0,27208-38-4
benzamide

: 72875-44-6
benzyl benzimidothioate

Guidance literature:: Multi-step reaction with 2 steps

1: Lawessons reagent / tetrahydrofuran / 12 h / 20 °C

2: chloroform / 12 h / Reflux

With Lawessons reagent; In tetrahydrofuran; chloroform;
DOI:10.1021/acs.jmedchem.7b00888