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1-(3-Phenoxypropyl)-4-phenylpiperazine

Base Information Edit
  • Chemical Name:1-(3-Phenoxypropyl)-4-phenylpiperazine
  • CAS No.:66307-58-2
  • Molecular Formula:C19H24N2O
  • Molecular Weight:296.412
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20216520
  • Nikkaji Number:J77.301H
  • Wikidata:Q83092752
  • Pharos Ligand ID:1XVV85TCK3RL
  • ChEMBL ID:CHEMBL1940414
  • Mol file:66307-58-2.mol
1-(3-Phenoxypropyl)-4-phenylpiperazine

Synonyms:1-(3-Phenoxypropyl)-4-phenylpiperazine;66307-58-2;Piperazine, 1-(3-phenoxypropyl)-4-phenyl-;CHEMBL1940414;DTXSID20216520;BDBM50362859;1-Phenoxy-3-(4-phenylpiperazino)propane;LS-113089

Suppliers and Price of 1-(3-Phenoxypropyl)-4-phenylpiperazine
Supply Marketing:Edit
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 1-(3-Phenoxypropyl)-4-phenylpiperazine Edit
Chemical Property:
  • Vapor Pressure:2.41E-08mmHg at 25°C 
  • Boiling Point:451.6°Cat760mmHg 
  • Flash Point:132.1°C 
  • PSA:15.71000 
  • Density:1.076g/cm3 
  • LogP:3.28060 
  • XLogP3:3.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:6
  • Exact Mass:296.188863393
  • Heavy Atom Count:22
  • Complexity:290
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CN(CCN1CCCOC2=CC=CC=C2)C3=CC=CC=C3
Technology Process of 1-(3-Phenoxypropyl)-4-phenylpiperazine

There total 8 articles about 1-(3-Phenoxypropyl)-4-phenylpiperazine 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:
Guidance literature:
With lithium carbonate; In acetonitrile; for 24h; Reflux; Inert atmosphere;
DOI:10.1016/j.ejmech.2011.04.032
Guidance literature:
With sodium carbonate; potassium iodide; In butan-1-ol; for 18h; Heating;
DOI:10.1021/jm00168a044
Guidance literature:
Multi-step reaction with 2 steps
1: triethylamine / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere
2: lithium carbonate / acetonitrile / 24 h / Reflux; Inert atmosphere
With lithium carbonate; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1016/j.ejmech.2011.04.032
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