4-Methyl-N-(1-phenylpentyl)benzene-1-sulfonamide

Base Information

Chemical Name:4-Methyl-N-(1-phenylpentyl)benzene-1-sulfonamide
CAS No.:124070-43-5
Molecular Formula:C18H23NO2S
Molecular Weight:317.452
Hs Code.:
DSSTox Substance ID:DTXSID30560960
Nikkaji Number:J274.708A
Mol file:124070-43-5.mol

Synonyms:124070-43-5;4-Methyl-N-(1-phenylpentyl)benzene-1-sulfonamide;DTXSID30560960

Suppliers and Price of 4-Methyl-N-(1-phenylpentyl)benzene-1-sulfonamide

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 2 raw suppliers

Chemical Property of 4-Methyl-N-(1-phenylpentyl)benzene-1-sulfonamide

Chemical Property:

XLogP3:4.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:317.14495015
Heavy Atom Count:22
Complexity:401

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 4-Methyl-N-(1-phenylpentyl)benzene-1-sulfonamide

There total 6 articles about 4-Methyl-N-(1-phenylpentyl)benzene-1-sulfonamide 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: 80.0%

: 542-69-8
1-iodo-butane

: 51608-60-7
phenyl N-tosyl imine

: 124070-43-5
4-methyl-N-(1-phenylpentyl)benzenesulfonamide

Guidance literature:: With air; boron trifluoride diethyl etherate; dimethyl zinc(II); copper(II) bis(trifluoromethanesulfonate); In hexane; dichloromethane; at 0 ℃; for 0.75h;
DOI:10.1021/ol052563r