Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

1-(4-(2-(2-propylamino)propyl)benzeneazo)piperidine

Base Information Edit
  • Chemical Name:1-(4-(2-(2-propylamino)propyl)benzeneazo)piperidine
  • CAS No.:123012-96-4
  • Molecular Formula:C17H28N4
  • Molecular Weight:288.436
  • Hs Code.:
  • Mol file:123012-96-4.mol
1-(4-(2-(2-propylamino)propyl)benzeneazo)piperidine

Synonyms:1-(4-(2-(2-propylamino)propyl)benzeneazo)piperidine

Suppliers and Price of 1-(4-(2-(2-propylamino)propyl)benzeneazo)piperidine
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-(4-(2-(2-propylamino)propyl)benzeneazo)piperidine Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 1-(4-(2-(2-propylamino)propyl)benzeneazo)piperidine

There total 8 articles about 1-(4-(2-(2-propylamino)propyl)benzeneazo)piperidine 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 potassium hydroxide; In ethanol; for 16h; Heating; in the dark;
Guidance literature:
Multi-step reaction with 5 steps
1: 96 percent / 4-dimethylaminopyridine / CH2Cl2 / 1.) 15 min, R.T., 2.) reflux, 1 h.
2: 1.) thallium(III) trifluoroacetate, 2.) amyl nitrite / 1.) trifluoroacetic acid, in the dark 75 h at R.T., 2.) dichloromethane, in the dark 3 h.
3: 93 percent / sodium borohydride / 10percent Pd/C / methanol / 1 h / Ambient temperature
4: 1.) 1M HCl, sodium nitrite / 1.) ethanol, water, 0-5 deg C, 10 min, 2.) 30 min.
5: 73 percent / 10percent potassium hydroxide / ethanol / 16 h / Heating; in the dark
With hydrogenchloride; dmap; potassium hydroxide; sodium tetrahydroborate; n-Amyl nitrite; sodium nitrite; thallium(III) trifluoroacetate; palladium on activated charcoal; In methanol; ethanol; dichloromethane;
Guidance literature:
Multi-step reaction with 6 steps
1: 95 percent / sodium borohydride / methanol / 14 h / Ambient temperature
2: 96 percent / 4-dimethylaminopyridine / CH2Cl2 / 1.) 15 min, R.T., 2.) reflux, 1 h.
3: 1.) thallium(III) trifluoroacetate, 2.) amyl nitrite / 1.) trifluoroacetic acid, in the dark 75 h at R.T., 2.) dichloromethane, in the dark 3 h.
4: 93 percent / sodium borohydride / 10percent Pd/C / methanol / 1 h / Ambient temperature
5: 1.) 1M HCl, sodium nitrite / 1.) ethanol, water, 0-5 deg C, 10 min, 2.) 30 min.
6: 73 percent / 10percent potassium hydroxide / ethanol / 16 h / Heating; in the dark
With hydrogenchloride; dmap; potassium hydroxide; sodium tetrahydroborate; n-Amyl nitrite; sodium nitrite; thallium(III) trifluoroacetate; palladium on activated charcoal; In methanol; ethanol; dichloromethane;
Post RFQ for Price