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N-(1H-benzimidazol-2-yl)-4-chlorobenzamide

Base Information
  • Chemical Name:N-(1H-benzimidazol-2-yl)-4-chlorobenzamide
  • CAS No.:55842-42-7
  • Molecular Formula:C14H10ClN3O
  • Molecular Weight:271.706
  • Hs Code.:
  • European Community (EC) Number:669-982-1
  • DSSTox Substance ID:DTXSID101324020
  • ChEMBL ID:CHEMBL486569
N-(1H-benzimidazol-2-yl)-4-chlorobenzamide

Synonyms:N-(1H-benzimidazol-2-yl)-4-chlorobenzamide;55842-42-7;N-(1H-benzo[d]imidazol-2-yl)-4-chlorobenzamide;CHEMBL486569;N-(1H-1,3-benzodiazol-2-yl)-4-chlorobenzamide;MLS001174612;SCHEMBL11206434;DTXSID101324020;HMS2897D04;BDBM50275235;STK443352;AKOS001055431;SMR000591547;EN300-16647541;N~1~-(1H-1,3-benzimidazol-2-yl)-4-chlorobenzamide;Z27666159

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Chemical Property of N-(1H-benzimidazol-2-yl)-4-chlorobenzamide
Chemical Property:
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:271.0512396
  • Heavy Atom Count:19
  • Complexity:331
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)NC(=N2)NC(=O)C3=CC=C(C=C3)Cl
Technology Process of N-(1H-benzimidazol-2-yl)-4-chlorobenzamide

There total 8 articles about N-(1H-benzimidazol-2-yl)-4-chlorobenzamide 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 pyridine; for 5h; Ambient temperature;
Guidance literature:
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 20 ℃;
DOI:10.1016/j.tetlet.2011.05.146
Guidance literature:
With 2-mesityl-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate; magnesium sulfate; potassium carbonate; lithium chloride; In tetrahydrofuran; at 20 ℃; for 48h;
DOI:10.1021/acs.orglett.7b01195
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