1-(p-ethylcarbamoylbenzenesulfonyl)-2-n-tridecyl-4-triphenylmethylpiperazine

Base Information

Chemical Name:1-(p-ethylcarbamoylbenzenesulfonyl)-2-n-tridecyl-4-triphenylmethylpiperazine
CAS No.:1027039-59-3
Molecular Formula:C₄₅H₅₉N₃O₄S
Molecular Weight:738.047
Hs Code.:

Synonyms:1-(p-ethylcarbamoylbenzenesulfonyl)-2-n-tridecyl-4-triphenylmethylpiperazine

Suppliers and Price of 1-(p-ethylcarbamoylbenzenesulfonyl)-2-n-tridecyl-4-triphenylmethylpiperazine

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 1-(p-ethylcarbamoylbenzenesulfonyl)-2-n-tridecyl-4-triphenylmethylpiperazine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-(p-ethylcarbamoylbenzenesulfonyl)-2-n-tridecyl-4-triphenylmethylpiperazine

There total 5 articles about 1-(p-ethylcarbamoylbenzenesulfonyl)-2-n-tridecyl-4-triphenylmethylpiperazine 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:

: 541-41-3
chloroformic acid ethyl ester

: 689286-40-6
1-(p-aminobenzenesulfonyl)-2-n-tridecyl-4-triphenylmethylpiperazine

: 1027039-59-3
1-(p-ethylcarbamoylbenzenesulfonyl)-2-n-tridecyl-4-triphenylmethylpiperazine

Guidance literature:: With triethylamine; In toluene; at 80 ℃; for 3h;
DOI:10.1016/S0223-5234(01)01274-0

Reference yield:

: 76-83-5
trityl chloride

: 1027039-59-3
1-(p-ethylcarbamoylbenzenesulfonyl)-2-n-tridecyl-4-triphenylmethylpiperazine

Guidance literature:: Multi-step reaction with 4 steps

1: 73 percent / triethylamine / CH₂Cl₂ / -13 °C

2: triethylamine / CH₂Cl₂ / 3 h / 20 °C

3: 17.8 g / KOH / ethanol / 48 h / Heating

4: triethylamine / toluene / 3 h / 80 °C

With potassium hydroxide; triethylamine; In ethanol; dichloromethane; toluene;
DOI:10.1016/S0223-5234(01)01274-0

Reference yield:

: 187228-89-3
1-triphenylmethyl-3-n-tridecylpiperazine

: 1027039-59-3
1-(p-ethylcarbamoylbenzenesulfonyl)-2-n-tridecyl-4-triphenylmethylpiperazine

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / CH₂Cl₂ / 3 h / 20 °C

2: 17.8 g / KOH / ethanol / 48 h / Heating

3: triethylamine / toluene / 3 h / 80 °C

With potassium hydroxide; triethylamine; In ethanol; dichloromethane; toluene;
DOI:10.1016/S0223-5234(01)01274-0