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Lodaxaprine

Base Information Edit
  • Chemical Name:Lodaxaprine
  • CAS No.:93181-81-8
  • Molecular Formula:C15H16ClN3O
  • Molecular Weight:289.76
  • Hs Code.:2933990090
  • Mol file:93181-81-8.mol
Lodaxaprine

Synonyms:1-(6-(2-Chlorophenyl)-3-pyridazinyl)-4-piperidinol;4-Piperidinol,1-(6-(2-chlorophenyl)-3-pyridazinyl);1-(6-(o-Chlorophenyl)-3-pyridazinyl)-4-piperidinol;3-(4-hydroxy-piperidino)-6-(2-chlorophenyl)pyridazine;Lodaxaprium [Latin];Lodaxaprine;Lodaxaprium;3-(4-Hydroxypiperidino)-6-(4-chlorophenyl)pyridazine;Lodaxaprina [Spanish];Lodaxaprina;

Suppliers and Price of Lodaxaprine
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
  • American Custom Chemicals Corporation
  • LODAXAPRINE 95.00%
  • 5MG
  • $ 500.93
Total 1 raw suppliers
Chemical Property of Lodaxaprine Edit
Chemical Property:
  • Vapor Pressure:7.16E-12mmHg at 25°C 
  • Boiling Point:525.5°Cat760mmHg 
  • Flash Point:271.6°C 
  • PSA:49.25000 
  • Density:1.303g/cm3 
  • LogP:2.82310 
Purity/Quality:

99% *data from raw suppliers

LODAXAPRINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of Lodaxaprine

There total 2 articles about Lodaxaprine 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:
In butan-1-ol; for 3h; Heating;
DOI:10.1021/jm00153a011
Guidance literature:
With triethylamine; In tetrahydrofuran; for 18h; Heating;
DOI:10.1021/jm00153a011
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