2-(2-((Z)-2-chlorostyryl)-5-nitro-1H-imidazol-1-yl)ethyl 4-methylbenzenesulfonate

Base Information

Chemical Name:2-(2-((Z)-2-chlorostyryl)-5-nitro-1H-imidazol-1-yl)ethyl 4-methylbenzenesulfonate
CAS No.:1609584-52-2
Molecular Formula:C₂₀H₁₈ClN₃O₅S
Molecular Weight:447.899
Hs Code.:

Synonyms:2-(2-((Z)-2-chlorostyryl)-5-nitro-1H-imidazol-1-yl)ethyl 4-methylbenzenesulfonate

Suppliers and Price of 2-(2-((Z)-2-chlorostyryl)-5-nitro-1H-imidazol-1-yl)ethyl 4-methylbenzenesulfonate

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of 2-(2-((Z)-2-chlorostyryl)-5-nitro-1H-imidazol-1-yl)ethyl 4-methylbenzenesulfonate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Technology Process of 2-(2-((Z)-2-chlorostyryl)-5-nitro-1H-imidazol-1-yl)ethyl 4-methylbenzenesulfonate

There total 3 articles about 2-(2-((Z)-2-chlorostyryl)-5-nitro-1H-imidazol-1-yl)ethyl 4-methylbenzenesulfonate 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: 77.2%

: 1609584-27-1
2-(2-((Z)-2-chlorostyryl)-5-nitro-1H-imidazol-1-yl)ethanol

: 98-59-9
p-toluenesulfonyl chloride

: 1609584-52-2
2-(2-((Z)-2-chlorostyryl)-5-nitro-1H-imidazol-1-yl)ethyl 4-methylbenzenesulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1016/j.ejmech.2014.07.082

Reference yield:

: 443-48-1
metronidazole

: 1609584-52-2
2-(2-((Z)-2-chlorostyryl)-5-nitro-1H-imidazol-1-yl)ethyl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium methylate / dimethyl sulfoxide; methanol / 4 h / 20 °C

2: triethylamine / dichloromethane / 5 h / 20 °C

With sodium methylate; triethylamine; In methanol; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/j.bmc.2014.04.005

Reference yield:

: 89-98-5
2-chloro-benzaldehyde

: 1609584-52-2
2-(2-((Z)-2-chlorostyryl)-5-nitro-1H-imidazol-1-yl)ethyl 4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium methylate / dimethyl sulfoxide; methanol / 4 h / 20 °C

2: triethylamine / dichloromethane / 5 h / 20 °C

With sodium methylate; triethylamine; In methanol; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/j.bmc.2014.04.005