N-[2-(4-Methylphenyl)prop-2-ene-1-sulfinyl]benzenesulfonamide

Base Information

Chemical Name:N-[2-(4-Methylphenyl)prop-2-ene-1-sulfinyl]benzenesulfonamide
CAS No.:88106-19-8
Molecular Formula:C16H17NO3S2
Molecular Weight:335.448
Hs Code.:
DSSTox Substance ID:DTXSID00555924

Synonyms:88106-19-8;DTXSID00555924;N-[2-(4-Methylphenyl)prop-2-ene-1-sulfinyl]benzenesulfonamide

Suppliers and Price of N-[2-(4-Methylphenyl)prop-2-ene-1-sulfinyl]benzenesulfonamide

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-(4-Methylphenyl)prop-2-ene-1-sulfinyl]benzenesulfonamide

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:335.06498575
Heavy Atom Count:22
Complexity:496

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C(=C)CS(=O)NS(=O)(=O)C2=CC=CC=C2

Technology Process of N-[2-(4-Methylphenyl)prop-2-ene-1-sulfinyl]benzenesulfonamide

There total 2 articles about N-[2-(4-Methylphenyl)prop-2-ene-1-sulfinyl]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%

: 6536-23-8
N-sulfinylbenzenesulfonamide

: 1195-32-0
1-methyl-4-isopropenylbenzene

: 88106-19-8
C₁₆H₁₇NO₃S₂

Guidance literature:: In diethyl ether; at 0 ℃; for 6h;
DOI:10.1021/jo00177a011

Reference yield:

: 98-10-2
benzenesulfonamide

: 88106-19-8
C₁₆H₁₇NO₃S₂

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / thionyl chloride, trimethylchlorosilane / benzene / Heating

2: 80 percent / diethyl ether / 6 h / 0 °C

With chloro-trimethyl-silane; thionyl chloride; In diethyl ether; benzene;
DOI:10.1016/S0040-4020(01)86670-9