4-[(2-butyl-5-nitro-1-benzofuran-3-yl)carbonyl]phenyl-4-nitrobenzenesulfonate

Base Information

Chemical Name:4-[(2-butyl-5-nitro-1-benzofuran-3-yl)carbonyl]phenyl-4-nitrobenzenesulfonate
CAS No.:1448297-20-8
Molecular Formula:C₂₅H₂₀N₂O₉S
Molecular Weight:524.508
Hs Code.:

Synonyms:4-[(2-butyl-5-nitro-1-benzofuran-3-yl)carbonyl]phenyl-4-nitrobenzenesulfonate

Suppliers and Price of 4-[(2-butyl-5-nitro-1-benzofuran-3-yl)carbonyl]phenyl-4-nitrobenzenesulfonate

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 4-[(2-butyl-5-nitro-1-benzofuran-3-yl)carbonyl]phenyl-4-nitrobenzenesulfonate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-[(2-butyl-5-nitro-1-benzofuran-3-yl)carbonyl]phenyl-4-nitrobenzenesulfonate

There total 1 articles about 4-[(2-butyl-5-nitro-1-benzofuran-3-yl)carbonyl]phenyl-4-nitrobenzenesulfonate 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:

: 141645-16-1
2-n-butyl-3-(4-hydroxybenzoyl)-5-nitrobenzofuran

: 98-74-8
4-Nitrobenzenesulfonyl chloride

: 1448297-20-8
4-[(2-butyl-5-nitro-1-benzofuran-3-yl)carbonyl]phenyl-4-nitrobenzenesulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 5.5h; Reflux;

Reference yield:

: 1448297-20-8
4-[(2-butyl-5-nitro-1-benzofuran-3-yl)carbonyl]phenyl-4-nitrobenzenesulfonate

: 141626-36-0
dronedarone

Guidance literature:: Multi-step reaction with 3 steps

1: palladium 10% on activated carbon; hydrogen / ethanol / 7 h / 75 °C / 7500.75 Torr

2: pyridine / dichloromethane / 5 h / 30 - 35 °C

3: potassium hydroxide / N,N-dimethyl-formamide / 9 h / 40 °C

With pyridine; palladium 10% on activated carbon; hydrogen; potassium hydroxide; In ethanol; dichloromethane; N,N-dimethyl-formamide;