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

Encyclopedia

Propanamide, N-(3,4-dichlorophenyl)-N-(2-(dimethylamino)cyclopentyl)-, cis-

Base Information Edit
  • Chemical Name:Propanamide, N-(3,4-dichlorophenyl)-N-(2-(dimethylamino)cyclopentyl)-, cis-
  • CAS No.:67450-78-6
  • Molecular Formula:C16H22Cl2N2O
  • Molecular Weight:329.269
  • Hs Code.:
  • DSSTox Substance ID:DTXSID001136933
  • Mol file:67450-78-6.mol
Propanamide, N-(3,4-dichlorophenyl)-N-(2-(dimethylamino)cyclopentyl)-, cis-

Synonyms:DCDPP;N-(2-(dimethylamino)cyclopentyl)-N-(3,4-dichlorophenyl)propanamid;U 78753E;U 78753E maleate;U 78753E, ethanedioate salt (1:1), (cis)-isomer;U-78753E

Suppliers and Price of Propanamide, N-(3,4-dichlorophenyl)-N-(2-(dimethylamino)cyclopentyl)-, cis-
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 Propanamide, N-(3,4-dichlorophenyl)-N-(2-(dimethylamino)cyclopentyl)-, cis- Edit
Chemical Property:
  • Boiling Point:443.5°Cat760mmHg 
  • Flash Point:222.1°C 
  • Density:1.22g/cm3 
  • XLogP3:4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:328.1109187
  • Heavy Atom Count:21
  • Complexity:364
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCC(=O)N(C1CCCC1N(C)C)C2=CC(=C(C=C2)Cl)Cl
  • Isomeric SMILES:CCC(=O)N([C@@H]1CCC[C@@H]1N(C)C)C2=CC(=C(C=C2)Cl)Cl
Technology Process of Propanamide, N-(3,4-dichlorophenyl)-N-(2-(dimethylamino)cyclopentyl)-, cis-

There total 10 articles about Propanamide, N-(3,4-dichlorophenyl)-N-(2-(dimethylamino)cyclopentyl)-, cis- 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:
Multi-step reaction with 5 steps
1: concd. HCl / 168 h / Heating
2: 72 h / Heating
3: 85percent aq. ethanolic KOH / 3 h / Ambient temperature
4: CrO3, aq. H2SO4 / acetone / 0.5 h / Ambient temperature
5: 4.2 g / dimethylamine hydrochloride, NaCNBH3 / methanol / 192 h / Ambient temperature
With chromium(VI) oxide; hydrogenchloride; potassium hydroxide; sulfuric acid; N,N-dimethylammonium chloride; sodium cyanoborohydride; In methanol; acetone;
DOI:10.1021/jm00142a020
Guidance literature:
Multi-step reaction with 4 steps
1: 90 percent / H2O
2: 1.) NaH / 1.) THF, reflux, 1 h
3: 2.) 20percent NaOH / 1.) reflux, 17 h, 2.) 1 h
4: Heating
With sodium hydroxide; sodium hydride; In water;
DOI:10.1021/jm00142a020
Guidance literature:
Multi-step reaction with 2 steps
1: CrO3, aq. H2SO4 / acetone / 0.5 h / Ambient temperature
2: 4.2 g / dimethylamine hydrochloride, NaCNBH3 / methanol / 192 h / Ambient temperature
With chromium(VI) oxide; sulfuric acid; N,N-dimethylammonium chloride; sodium cyanoborohydride; In methanol; acetone;
DOI:10.1021/jm00142a020
Post RFQ for Price