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N,4-diphenyl-1H-1,2,3-triazol-5-amine

Base Information
  • Chemical Name:N,4-diphenyl-1H-1,2,3-triazol-5-amine
  • CAS No.:53684-55-2
  • Molecular Formula:C14H12N4
  • Molecular Weight:236.276
  • Hs Code.:
  • European Community (EC) Number:688-681-6
  • DSSTox Substance ID:DTXSID40423294
  • Wikidata:Q82235478
  • ChEMBL ID:CHEMBL1345333
N,4-diphenyl-1H-1,2,3-triazol-5-amine

Synonyms:N,4-diphenyl-1H-1,2,3-triazol-5-amine;53684-55-2;N,5-diphenyl-2H-triazol-4-amine;MLS000105068;Cambridge id 5140720;Oprea1_459787;SCHEMBL2491021;CHEMBL1345333;DTXSID40423294;HMS2344E18;N,5-diphenyl-3H-triazol-4-amine;CCG-2183;AKOS003627258;SMR000054997;N,5-diphenyl-2H-1,2,3-triazol-4-amine;FT-0657999;1H-1,2,3-Triazol-5-amine, N,4-diphenyl-;AB00074348-01;A829732

Suppliers and Price of N,4-diphenyl-1H-1,2,3-triazol-5-amine
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 7 raw suppliers
Chemical Property of N,4-diphenyl-1H-1,2,3-triazol-5-amine
Chemical Property:
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:236.106196400
  • Heavy Atom Count:18
  • Complexity:246
Purity/Quality:

98%Min *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C2=NNN=C2NC3=CC=CC=C3
Technology Process of N,4-diphenyl-1H-1,2,3-triazol-5-amine

There total 7 articles about N,4-diphenyl-1H-1,2,3-triazol-5-amine 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 tert-butylate; In neat (no solvent); at 150 - 180 ℃; for 6h; Sealed tube;
DOI:10.1002/ejoc.202001620
Guidance literature:
Multi-step reaction with 2 steps
1: sodium methylate
2: 184 - 185 °C
With sodium methylate;
DOI:10.1021/jo01357a018
Guidance literature:
Multi-step reaction with 2 steps
1: potassium tert-butylate / neat (no solvent) / 24 h / 25 °C / Sealed tube
2: potassium tert-butylate / neat (no solvent) / 6 h / 150 - 180 °C / Sealed tube
With potassium tert-butylate; In neat (no solvent); 2: |Dimroth Rearrangement;
DOI:10.1002/ejoc.202001620
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