N-(2-Methyl-2-propenyl)-N-tosylaniline

Base Information

Chemical Name:N-(2-Methyl-2-propenyl)-N-tosylaniline
CAS No.:87929-22-4
Molecular Formula:C17H19NO2S
Molecular Weight:301.409
Hs Code.:
DSSTox Substance ID:DTXSID60399189
Nikkaji Number:J1.819.291H
Wikidata:Q82201584

Synonyms:N-(2-Methyl-2-propenyl)-N-tosylaniline;ST51010328;87929-22-4;DTXSID60399189;AKOS024372565

Suppliers and Price of N-(2-Methyl-2-propenyl)-N-tosylaniline

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-(2-Methyl-2-propenyl)-N-tosylaniline

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:301.11365002
Heavy Atom Count:21
Complexity:438

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(CC(=C)C)C2=CC=CC=C2

Technology Process of N-(2-Methyl-2-propenyl)-N-tosylaniline

There total 5 articles about N-(2-Methyl-2-propenyl)-N-tosylaniline 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:

: 1458-98-6
2-methyl-3-bromo-1-propene

: 68-34-8
phenyl toluenesulfonamide

: 87929-22-4
4-methyl-N-(2-methylallyl)-N-phenylbenzenesulfonamide

Guidance literature:: With potassium carbonate; In acetone; Reflux;
DOI:10.1021/acscatal.6b02586

Reference yield:

: 62-53-3
aniline

: 87929-22-4
4-methyl-N-(2-methylallyl)-N-phenylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 22 °C

2: potassium carbonate / acetone / Reflux

With potassium carbonate; triethylamine; In dichloromethane; acetone;
DOI:10.1021/acscatal.6b02586

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 87929-22-4
4-methyl-N-(2-methylallyl)-N-phenylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 22 °C

2: potassium carbonate / acetone / Reflux

With potassium carbonate; triethylamine; In dichloromethane; acetone;
DOI:10.1021/acscatal.6b02586