4-Piperazin-1-yl-quinoline

Base Information

Chemical Name:4-Piperazin-1-yl-quinoline
CAS No.:118306-89-1
Molecular Formula:C13H15 N3
Molecular Weight:213.282
Hs Code.:
European Community (EC) Number:808-680-8
DSSTox Substance ID:DTXSID30364187
Nikkaji Number:J1.570.565E
Wikidata:Q82148005
ChEMBL ID:CHEMBL2441621
Mol file:118306-89-1.mol

Synonyms:4-Piperazin-1-yl-quinoline;118306-89-1;4-piperazin-1-ylquinoline;4-(piperazin-1-yl)quinoline;4-Piperazinylquinoline;1-(4-quinolinyl)piperazine;CHEMBL2441621;4-(1-PIPERAZINYL)QUINOLINE;1-(4-quinolyl)piperazine;SCHEMBL900231;DTXSID30364187;BDBM50520368;MFCD02179800;STL259592;AKOS000291550;BB 0239058;CS-0267683;FT-0706783;EN300-78038;J-003733

Suppliers and Price of 4-Piperazin-1-yl-quinoline

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
4-PIPERAZIN-1-YL-QUINOLINE 95.00%
5MG
$ 505.10

Chemenu
4-(Piperazin-1-yl)quinoline 95%
5g
$ 982.00

Chemenu
4-(Piperazin-1-yl)quinoline 95%
1g
$ 346.00

Total 9 raw suppliers

Chemical Property of 4-Piperazin-1-yl-quinoline

Chemical Property:

Vapor Pressure:9.98E-07mmHg at 25°C
Refractive Index:1.628
Boiling Point:403.7°C at 760 mmHg
PKA:10.14±0.46(Predicted)
Flash Point:198°C
PSA：28.16000
Density:1.152g/cm³
LogP:2.03820
XLogP3:0.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:213.126597491
Heavy Atom Count:16
Complexity:225

Purity/Quality:

97% ^*data from raw suppliers

4-PIPERAZIN-1-YL-QUINOLINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(CCN1)C2=CC=NC3=CC=CC=C32

Technology Process of 4-Piperazin-1-yl-quinoline

There total 4 articles about 4-Piperazin-1-yl-quinoline 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: 100.0%