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1H-Benzimidazole-5,6-diol

Base Information
  • Chemical Name:1H-Benzimidazole-5,6-diol
  • CAS No.:102169-73-3
  • Molecular Formula:C7H6 N2 O2
  • Molecular Weight:150.13
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10570244
  • Wikidata:Q82457629
  • Mol file:102169-73-3.mol
1H-Benzimidazole-5,6-diol

Synonyms:102169-73-3;1H-BENZIMIDAZOLE-5,6-DIOL;1H-BENZO[D]IMIDAZOLE-5,6-DIOL;Benzimidazole-5,6-diol;5,6-Dihydroxy-1H-benzimidazole;SCHEMBL2264663;SCHEMBL5266961;DTXSID10570244;1H-Benzimidazole-5,6-diol(9CI);AMY24261;MFCD18807895;SY262936

Suppliers and Price of 1H-Benzimidazole-5,6-diol
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
  • Alichem
  • 5,6-Dihydroxy-1H-benzimidazole
  • 500mg
  • $ 1107.89
  • Alichem
  • 5,6-Dihydroxy-1H-benzimidazole
  • 250mg
  • $ 849.66
  • Alichem
  • 5,6-Dihydroxy-1H-benzimidazole
  • 1g
  • $ 1979.21
  • AK Scientific
  • 1H-Benzimidazole-5,6-diol
  • 1g
  • $ 1747.00
Total 1 raw suppliers
Chemical Property of 1H-Benzimidazole-5,6-diol
Chemical Property:
  • Boiling Point:548.0±30.0 °C(Predicted) 
  • PKA:8.65±0.40(Predicted) 
  • PSA:69.14000 
  • Density:1.632±0.06 g/cm3(Predicted) 
  • LogP:0.97410 
  • XLogP3:0.8
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:150.042927438
  • Heavy Atom Count:11
  • Complexity:153
Purity/Quality:

5,6-Dihydroxy-1H-benzimidazole *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=C2C(=CC(=C1O)O)N=CN2
Technology Process of 1H-Benzimidazole-5,6-diol

There total 4 articles about 1H-Benzimidazole-5,6-diol 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 hydrogen bromide; at 100 ℃; for 8h;
DOI:10.1039/c5ra25590b
Guidance literature:
Multi-step reaction with 4 steps
1: nitric acid / 2 h / 0 - 80 °C
2: hydrazine hydrate; palladium on activated charcoal
3: 2 h / 100 °C
4: hydrogen bromide / 8 h / 100 °C
With palladium on activated charcoal; hydrogen bromide; nitric acid; hydrazine hydrate;
DOI:10.1039/c5ra25590b
Guidance literature:
Multi-step reaction with 3 steps
1: hydrazine hydrate; palladium on activated charcoal
2: 2 h / 100 °C
3: hydrogen bromide / 8 h / 100 °C
With palladium on activated charcoal; hydrogen bromide; hydrazine hydrate;
DOI:10.1039/c5ra25590b
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