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5-(Dimethylamino)-2,1,3-benzoxadiazole

Base Information Edit
  • Chemical Name:5-(Dimethylamino)-2,1,3-benzoxadiazole
  • CAS No.:6124-22-7
  • Molecular Formula:C8H9N3O
  • Molecular Weight:163.17700
  • Hs Code.:2934999090
  • Mol file:6124-22-7.mol
5-(Dimethylamino)-2,1,3-benzoxadiazole

Synonyms:5-Dimethylamino-benzofurazan;2,1,3-Benzoxadiazol-5-amine,N,N-dimethyl;

Suppliers and Price of 5-(Dimethylamino)-2,1,3-benzoxadiazole
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 2 raw suppliers
Chemical Property of 5-(Dimethylamino)-2,1,3-benzoxadiazole Edit
Chemical Property:
  • PSA:42.16000 
  • LogP:1.28880 
Purity/Quality:

95% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 5-(Dimethylamino)-2,1,3-benzoxadiazole

There total 7 articles about 5-(Dimethylamino)-2,1,3-benzoxadiazole 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 water; acetonitrile; at 20 ℃; for 72h;
DOI:10.1039/b202367a
Guidance literature:
With triethyl phosphite; In ethanol;
DOI:10.1021/jm00308a027
Guidance literature:
Multi-step reaction with 3 steps
1: 84 percent / potassium hydroxide; sodium hypochlorite / ethanol; H2O / 0.33 h / 20 °C
2: triphenylphosphine / chlorobenzene / 0.33 h / 20 °C
3: 69 percent / acetonitrile; H2O / 72 h / 20 °C
With potassium hydroxide; sodium hypochlorite; triphenylphosphine; In ethanol; water; chlorobenzene; acetonitrile;
DOI:10.1039/b202367a
Refernces Edit
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