4-chloro-N-ethyl-N-(2-methylphenyl)benzenesulfonamide

Base Information

Chemical Name:4-chloro-N-ethyl-N-(2-methylphenyl)benzenesulfonamide
CAS No.:14417-04-0
Molecular Formula:C₁₅H₁₆ClNO₂S
Molecular Weight:309.817
Hs Code.:
DSSTox Substance ID:DTXSID301213411

Synonyms:4-chloro-N-ethyl-N-(2-methylphenyl)benzenesulfonamide;SCHEMBL17174234;DTXSID301213411;AKOS002786691;Z45541545;14417-04-0

Suppliers and Price of 4-chloro-N-ethyl-N-(2-methylphenyl)benzenesulfonamide

Supply Marketing:

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

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Chemical Property of 4-chloro-N-ethyl-N-(2-methylphenyl)benzenesulfonamide

Chemical Property:

XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:309.0590276
Heavy Atom Count:20
Complexity:399

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCN(C1=CC=CC=C1C)S(=O)(=O)C2=CC=C(C=C2)Cl

Technology Process of 4-chloro-N-ethyl-N-(2-methylphenyl)benzenesulfonamide

There total 3 articles about 4-chloro-N-ethyl-N-(2-methylphenyl)benzenesulfonamide 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: 81.0%

: 7454-46-8
N-(2-methylphenyl)-4-chlorobenzene sulfonamide

: 75-03-6
ethyl iodide

: 14417-04-0
N-(2-methylphenyl)-N-ethyl-4-chlorobenzenesulfonamide

Guidance literature:: N-(2-methylphenyl)-4-chlorobenzene sulfonamide; With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;

ethyl iodide; In N,N-dimethyl-formamide;

Reference yield:

: 95-53-4
o-toluidine

: 14417-04-0
N-(2-methylphenyl)-N-ethyl-4-chlorobenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium carbonate / water / pH 9 - 10

2: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 20 °C

With sodium hydride; sodium carbonate; In water; N,N-dimethyl-formamide;

Reference yield:

: 98-60-2
4-chlorobenzenesulfonyl chloride

: 14417-04-0
N-(2-methylphenyl)-N-ethyl-4-chlorobenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium carbonate / water / pH 9 - 10

2: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 20 °C

With sodium hydride; sodium carbonate; In water; N,N-dimethyl-formamide;