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4-(2H-tetrazol-5-yl)benzamide

Base Information
  • Chemical Name:4-(2H-tetrazol-5-yl)benzamide
  • CAS No.:92712-51-1
  • Molecular Formula:C8H7N5O
  • Molecular Weight:189.176
  • Hs Code.:
  • European Community (EC) Number:872-319-0
  • Nikkaji Number:J1.494.735C
4-(2H-tetrazol-5-yl)benzamide

Synonyms:4-(2H-tetrazol-5-yl)benzamide;92712-51-1;4-(2H-1,2,3,4-tetrazol-5-yl)benzamide;Benzamide, 4-(1H-tetrazol-5-yl)-;SCHEMBL751010;SCHEMBL17963197;4-(1H-Tetrazole-5-yl)benzamide;MFCD04035672;AKOS008997037;AKOS027439846;EN300-14534;Z104341536

Suppliers and Price of 4-(2H-tetrazol-5-yl)benzamide
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 4 raw suppliers
Chemical Property of 4-(2H-tetrazol-5-yl)benzamide
Chemical Property:
  • XLogP3:0
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:189.06505986
  • Heavy Atom Count:14
  • Complexity:214
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC(=CC=C1C2=NNN=N2)C(=O)N
Technology Process of 4-(2H-tetrazol-5-yl)benzamide

There total 1 articles about 4-(2H-tetrazol-5-yl)benzamide 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 sodium azide; ammonium chloride; In N,N-dimethyl-formamide; at 100 - 110 ℃; for 18h;
DOI:10.1021/jm00386a019
Guidance literature:
With triethylamine; In N,N-dimethyl-formamide; at 20 - 25 ℃; for 3h;
DOI:10.1021/jm00386a019
Guidance literature:
Multi-step reaction with 2 steps
1: Et3N / dimethylformamide / 3 h / 20 - 25 °C
2: 37 percent / morpholine-iodine complex / benzene / 16 h / 20 - 25 °C
With triethylamine; morpholine-iodine complex; In N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00386a019
upstream raw materials:

4-cyanobenzamide

Downstream raw materials:

2-(1'-iodopropyn-3'-yl)-5-(p-carbamoylphenyl)tetrazole

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