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N-1-BENZYL-3-BENZYL-PIPERAZINE

Base Information Edit
  • Chemical Name:N-1-BENZYL-3-BENZYL-PIPERAZINE
  • CAS No.:179051-52-6
  • Molecular Formula:C18H22 N2
  • Molecular Weight:266.386
  • Hs Code.:
  • Mol file:179051-52-6.mol
N-1-BENZYL-3-BENZYL-PIPERAZINE

Synonyms:1,3-Dibenzylpiperazine

Suppliers and Price of N-1-BENZYL-3-BENZYL-PIPERAZINE
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
  • Ambeed
  • N-1-benzyl-3-benzyl-piperazine 97%
  • 1g
  • $ 294.00
  • Ambeed
  • N-1-benzyl-3-benzyl-piperazine 97%
  • 250mg
  • $ 121.00
  • Ambeed
  • N-1-benzyl-3-benzyl-piperazine 97%
  • 100mg
  • $ 77.00
Total 6 raw suppliers
Chemical Property of N-1-BENZYL-3-BENZYL-PIPERAZINE Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Refractive Index:1.584 
  • Boiling Point:391.5°Cat760mmHg 
  • PKA:9.25±0.40(Predicted) 
  • Flash Point:149.1°C 
  • PSA:15.27000 
  • Density:1.064g/cm3 
  • LogP:2.96980 
Purity/Quality:

98%Min *data from raw suppliers

N-1-benzyl-3-benzyl-piperazine 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of N-1-BENZYL-3-BENZYL-PIPERAZINE

There total 4 articles about N-1-BENZYL-3-BENZYL-PIPERAZINE 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:
1-benzyl-3-(R)-benzyl piperazine-2,5-dione; With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 21.75h; Heating / reflux;
With sodium hydroxide; water; In tetrahydrofuran;
Guidance literature:
Multi-step reaction with 2 steps
1.1: thionyl chloride / methanol / 2.5 h / 0 - 20 °C
1.2: 18 h
2.1: lithium aluminium tetrahydride / tetrahydrofuran / 21.75 h / 0 °C / Heating / reflux
With lithium aluminium tetrahydride; thionyl chloride; In tetrahydrofuran; methanol;
Guidance literature:
Multi-step reaction with 3 steps
1.1: 2,3,4,5,6-pentafluorophenol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 1 h / 20 °C
1.2: 20 h / 20 °C
2.1: thionyl chloride / methanol / 2.5 h / 0 - 20 °C
2.2: 18 h
3.1: lithium aluminium tetrahydride / tetrahydrofuran / 21.75 h / 0 °C / Heating / reflux
With lithium aluminium tetrahydride; thionyl chloride; 2,3,4,5,6-pentafluorophenol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; methanol; dichloromethane;
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