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4-(4-Aminobenzyl)-N-ethylaniline

Base Information Edit
  • Chemical Name:4-(4-Aminobenzyl)-N-ethylaniline
  • CAS No.:51947-46-7
  • Molecular Formula:C15H18 N2
  • Molecular Weight:226.321
  • Hs Code.:2921590090
  • European Community (EC) Number:257-540-7
  • DSSTox Substance ID:DTXSID00199923
  • Nikkaji Number:J279.384I
  • Wikidata:Q83072947
  • Mol file:51947-46-7.mol
4-(4-Aminobenzyl)-N-ethylaniline

Synonyms:4-(4-Aminobenzyl)-N-ethylaniline;51947-46-7;EINECS 257-540-7;DTXSID00199923;Ethyl-(4-p-aminotolyl)-phenyl-amine;4-[(4-Aminophenyl)methyl]-N-ethylaniline;Benzenamine, 4-((4-aminophenyl)methyl)-N-ethyl-

Suppliers and Price of 4-(4-Aminobenzyl)-N-ethylaniline
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 3 raw suppliers
Chemical Property of 4-(4-Aminobenzyl)-N-ethylaniline Edit
Chemical Property:
  • Vapor Pressure:1.1E-06mmHg at 25°C 
  • Boiling Point:402.4°Cat760mmHg 
  • Flash Point:233.1°C 
  • PSA:38.05000 
  • Density:1.092g/cm3 
  • LogP:3.94560 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:226.146998583
  • Heavy Atom Count:17
  • Complexity:201
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCNC1=CC=C(C=C1)CC2=CC=C(C=C2)N
Technology Process of 4-(4-Aminobenzyl)-N-ethylaniline

There total 1 articles about 4-(4-Aminobenzyl)-N-ethylaniline 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 tetrahydrofuran; diethyl ether; 1.) room temperature, 12 h, 2.) 50 deg C, 12 h;
Refernces Edit
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