Benzenesulfonamide, N-(4-iodophenyl)-N,4-dimethyl-

Base Information

Chemical Name:Benzenesulfonamide, N-(4-iodophenyl)-N,4-dimethyl-
CAS No.:327060-00-4
Molecular Formula:C14H14INO2S
Molecular Weight:387.241
Hs Code.:
DSSTox Substance ID:DTXSID40453233
Nikkaji Number:J2.223.742J
Wikidata:Q82274333

Synonyms:Benzenesulfonamide, N-(4-iodophenyl)-N,4-dimethyl-;327060-00-4;DTXSID40453233;1-Iodo-4-(methyltosylamino)benzene

Suppliers and Price of Benzenesulfonamide, N-(4-iodophenyl)-N,4-dimethyl-

Supply Marketing:

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

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Chemical Property of Benzenesulfonamide, N-(4-iodophenyl)-N,4-dimethyl-

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:386.97900
Heavy Atom Count:19
Complexity:377

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)N(C)C2=CC=C(C=C2)I

Technology Process of Benzenesulfonamide, N-(4-iodophenyl)-N,4-dimethyl-

There total 4 articles about Benzenesulfonamide, N-(4-iodophenyl)-N,4-dimethyl- 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: 90.0%

: 158268-30-5
N-tosyl-4-iodoaniline

: 74-88-4
methyl iodide

: 327060-00-4
N-methyl-N-(4-iodo-phenyl)-4-methyl-benzenesulfonamide

Guidance literature:: With PS-BEMP; In N,N-dimethyl-formamide; at 20 ℃; for 18h;
DOI:10.1039/b313414h

Reference yield: 90.0%

: 158268-30-5
N-tosyl-4-iodoaniline

: 327060-00-4
N-methyl-N-(4-iodo-phenyl)-4-methyl-benzenesulfonamide

Guidance literature:: With polymer-supported Schwesinger base PS-BEMP; In N,N-dimethyl-formamide; at 20 ℃; for 18h;
DOI:10.1039/b305713e

Reference yield:

: 540-37-4
p-aminoiodobenzene

: 327060-00-4
N-methyl-N-(4-iodo-phenyl)-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 4 h / 85 °C

2: 1.75 g / K₂CO₃ / dimethylformamide / 48 h

With pyridine; potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1021/ol051947e