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N1-[3-(Dimethylamino)propyl]benzene-1,2-diamine

Base Information
  • Chemical Name:N1-[3-(Dimethylamino)propyl]benzene-1,2-diamine
  • CAS No.:21627-59-8
  • Molecular Formula:C11H19N3
  • Molecular Weight:193.292
  • Hs Code.:2921590090
  • DSSTox Substance ID:DTXSID30556944
  • Wikidata:Q82438673
  • Mol file:21627-59-8.mol
N1-[3-(Dimethylamino)propyl]benzene-1,2-diamine

Synonyms:21627-59-8;N1-[3-(DIMETHYLAMINO)PROPYL]BENZENE-1,2-DIAMINE;n1-(3-(dimethylamino)propyl)benzene-1,2-diamine;SCHEMBL974271;DTXSID30556944;LDOZLAKDJCZQKM-UHFFFAOYSA-N;MFCD10699312;AKOS009236516;2-(3-dimethylaminopropylamino)-aniline;N-[3-(dimethylamino)propyl]-1,2-benzenediamine;N~1~-[3-(Dimethylamino)propyl]benzene-1,2-diamine;F1911-3679

Suppliers and Price of N1-[3-(Dimethylamino)propyl]benzene-1,2-diamine
Supply Marketing:
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 N1-[3-(Dimethylamino)propyl]benzene-1,2-diamine
Chemical Property:
  • PSA:41.29000 
  • LogP:2.28660 
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:193.157897619
  • Heavy Atom Count:14
  • Complexity:148
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CN(C)CCCNC1=CC=CC=C1N
Technology Process of N1-[3-(Dimethylamino)propyl]benzene-1,2-diamine

There total 5 articles about N1-[3-(Dimethylamino)propyl]benzene-1,2-diamine 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 5%-palladium/activated carbon; hydrogen; In ethanol; at 20 ℃; Sealed tube;
DOI:10.3390/molecules26144200
Guidance literature:
Multi-step reaction with 2 steps
1: ethanol / 24 h / Heating
2: H2 / 5percent Pd/C / ethanol
With hydrogen; palladium on activated charcoal; In ethanol;
Guidance literature:
Multi-step reaction with 2 steps
1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 18 h / 60 °C
2: ammonium formate; zinc / ethanol / 2 h / 60 °C
With ammonium formate; N-ethyl-N,N-diisopropylamine; zinc; In ethanol; dimethyl sulfoxide;
DOI:10.1016/j.bmcl.2011.10.029
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