Piperidine, 1-[(4-methylphenyl)sulfonyl]-2-(2-oxo-2-phenylethyl)-

Base Information

Chemical Name:Piperidine, 1-[(4-methylphenyl)sulfonyl]-2-(2-oxo-2-phenylethyl)-
CAS No.:89881-44-7
Molecular Formula:C20H23NO3S
Molecular Weight:357.474
Hs Code.:
DSSTox Substance ID:DTXSID00472945
Nikkaji Number:J1.099.488H

Synonyms:89881-44-7;Piperidine, 1-[(4-methylphenyl)sulfonyl]-2-(2-oxo-2-phenylethyl)-;DTXSID00472945

Suppliers and Price of Piperidine, 1-[(4-methylphenyl)sulfonyl]-2-(2-oxo-2-phenylethyl)-

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 0 raw suppliers

Chemical Property of Piperidine, 1-[(4-methylphenyl)sulfonyl]-2-(2-oxo-2-phenylethyl)-

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:357.13986477
Heavy Atom Count:25
Complexity:540

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)N2CCCCC2CC(=O)C3=CC=CC=C3

Technology Process of Piperidine, 1-[(4-methylphenyl)sulfonyl]-2-(2-oxo-2-phenylethyl)-

There total 3 articles about Piperidine, 1-[(4-methylphenyl)sulfonyl]-2-(2-oxo-2-phenylethyl)- 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%

: N-(5-hydroxy-7-phenylhept-6-yn-1-yl)-4-methylbenzenesulfonamide

: 89881-44-7
2-(1-(4-methylbenzenesulfonyl)-2-pyperidinyl)-1-phenylethanone

Guidance literature:: With [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I) (2:1) toluene adduct; In methanol; toluene; at 20 ℃; for 24h;
DOI:10.1016/j.tetlet.2015.09.115

Reference yield: 61.0%

: 70-55-3
toluene-4-sulfonamide

: 227018-70-4
(E)-7-iodo-1-phenyl-2-hepten-1-one

: 89881-44-7
2-(1-(4-methylbenzenesulfonyl)-2-pyperidinyl)-1-phenylethanone

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; for 24h; Ambient temperature;
DOI:10.1080/00397919908086214

Reference yield:

: 227018-67-9
(E)-7-chloro-1-phenyl-2-hepten-1-one

: 89881-44-7
2-(1-(4-methylbenzenesulfonyl)-2-pyperidinyl)-1-phenylethanone

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / NaI / acetone / 24 h / Heating

2: 61 percent / K₂CO₃ / dimethylformamide / 24 h / Ambient temperature

With potassium carbonate; sodium iodide; In N,N-dimethyl-formamide; acetone;
DOI:10.1080/00397919908086214