N-[(3E)-2,2-dichloro-1-(4-chlorophenyl)-3-(cyclohexylimino)-3-phenylpropyl]phenylsulfonamide

Base Information

Chemical Name:N-[(3E)-2,2-dichloro-1-(4-chlorophenyl)-3-(cyclohexylimino)-3-phenylpropyl]phenylsulfonamide
CAS No.:907563-71-7
Molecular Formula:C₂₇H₂₇Cl₃N₂O₂S
Molecular Weight:549.949
Hs Code.:

Synonyms:N-[(3E)-2,2-dichloro-1-(4-chlorophenyl)-3-(cyclohexylimino)-3-phenylpropyl]phenylsulfonamide

Suppliers and Price of N-[(3E)-2,2-dichloro-1-(4-chlorophenyl)-3-(cyclohexylimino)-3-phenylpropyl]phenylsulfonamide

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 N-[(3E)-2,2-dichloro-1-(4-chlorophenyl)-3-(cyclohexylimino)-3-phenylpropyl]phenylsulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-[(3E)-2,2-dichloro-1-(4-chlorophenyl)-3-(cyclohexylimino)-3-phenylpropyl]phenylsulfonamide

There total 5 articles about N-[(3E)-2,2-dichloro-1-(4-chlorophenyl)-3-(cyclohexylimino)-3-phenylpropyl]phenylsulfonamide 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: 47.0%

: 907563-66-0
N-(2,2-dichloro-1-phenylethylidene)cyclohexylamine

: 664986-03-2
(E)-N-(4-chlorobenzylidene)benzenesulfonamide

: 907563-71-7
N-[(3E)-2,2-dichloro-1-(4-chlorophenyl)-3-(cyclohexylimino)-3-phenylpropyl]phenylsulfonamide

Guidance literature:: N-(2,2-dichloro-1-phenylethylidene)cyclohexylamine; With lithium diisopropyl amide; In tetrahydrofuran; hexane; at 0 ℃; for 0.5h;

(E)-N-(4-chlorobenzylidene)benzenesulfonamide; In tetrahydrofuran; hexane; at -40 - 20 ℃; for 14h;
DOI:10.1021/jo060241a

Reference yield:

: 98-10-2
benzenesulfonamide

: 907563-71-7
N-[(3E)-2,2-dichloro-1-(4-chlorophenyl)-3-(cyclohexylimino)-3-phenylpropyl]phenylsulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 170 °C

2.1: lithium diisopropylamide / tetrahydrofuran; hexane / 0.5 h / 0 °C

2.2: 47 percent / tetrahydrofuran; hexane / 14 h / -40 - 20 °C

With lithium diisopropyl amide; In tetrahydrofuran; hexane;
DOI:10.1021/jo060241a

Reference yield:

: 2648-61-5
2,2-dichloroacetophenone

: 907563-71-7
N-[(3E)-2,2-dichloro-1-(4-chlorophenyl)-3-(cyclohexylimino)-3-phenylpropyl]phenylsulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 75 percent / TiCl₄ / diethyl ether; pentane / 0 - 20 °C

2.1: lithium diisopropylamide / tetrahydrofuran; hexane / 0.5 h / 0 °C

2.2: 47 percent / tetrahydrofuran; hexane / 14 h / -40 - 20 °C

With titanium tetrachloride; lithium diisopropyl amide; In tetrahydrofuran; diethyl ether; hexane; pentane;
DOI:10.1021/jo060241a