Quinoline, 2,8-dimethyl-4-(p-(4-(o-tolyl)-1-piperazinyl)anilino)-

Base Information

Chemical Name:Quinoline, 2,8-dimethyl-4-(p-(4-(o-tolyl)-1-piperazinyl)anilino)-
CAS No.:87602-50-4
Molecular Formula:C28H30 N4
Molecular Weight:0
Hs Code.:2933990090
DSSTox Substance ID:DTXSID50236519
Wikidata:Q83118490
Mol file:87602-50-4.mol

Synonyms:BRN 6009547;2,8-Dimethyl-4-(p-(4-(o-tolyl)-1-piperazinyl)anilino)quinoline;Quinoline, 2,8-dimethyl-4-(p-(4-(o-tolyl)-1-piperazinyl)anilino)-;87602-50-4;4-Quinolinamine, 2,8-dimethyl-N-(4-(4-(2-methylphenyl)-1-piperazinyl)phenyl)-;DTXSID50236519;LS-141906

Suppliers and Price of Quinoline, 2,8-dimethyl-4-(p-(4-(o-tolyl)-1-piperazinyl)anilino)-

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

American Custom Chemicals Corporation
2,8-DIMETHYL-4-(P-(4-(O-TOLYL)-1-PIPERAZINYL)ANILINO)QUINOLINE 95.00%
5MG
$ 503.17

Total 3 raw suppliers

Chemical Property of Quinoline, 2,8-dimethyl-4-(p-(4-(o-tolyl)-1-piperazinyl)anilino)-

Chemical Property:

Vapor Pressure:1.09E-14mmHg at 25°C
Boiling Point:607.2°C at 760 mmHg
Flash Point:321°C
PSA：34.63000
Density:1.176g/cm³
LogP:5.78210
XLogP3:6.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:422.24704697
Heavy Atom Count:32
Complexity:580

Purity/Quality:: 2,8-DIMETHYL-4-(P-(4-(O-TOLYL)-1-PIPERAZINYL)ANILINO)QUINOLINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C2C(=CC=C1)C(=CC(=N2)C)NC3=CC=C(C=C3)N4CCN(CC4)C5=CC=CC=C5C

Technology Process of Quinoline, 2,8-dimethyl-4-(p-(4-(o-tolyl)-1-piperazinyl)anilino)-

There total 1 articles about Quinoline, 2,8-dimethyl-4-(p-(4-(o-tolyl)-1-piperazinyl)anilino)- 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: 82.0%