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2-Amino-4-azido-3,5,6-trifluorobenzoic acid

Base Information
  • Chemical Name:2-Amino-4-azido-3,5,6-trifluorobenzoic acid
  • CAS No.:126695-67-8
  • Molecular Formula:C7H3F3N4O2
  • Molecular Weight:232.122
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40562511
  • Nikkaji Number:J323.738I
  • Wikidata:Q82446705
  • Mol file:126695-67-8.mol
2-Amino-4-azido-3,5,6-trifluorobenzoic acid

Synonyms:2-Amino-4-azido-3,5,6-trifluorobenzoic acid;126695-67-8;DTXSID40562511

Suppliers and Price of 2-Amino-4-azido-3,5,6-trifluorobenzoic acid
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 2 raw suppliers
Chemical Property of 2-Amino-4-azido-3,5,6-trifluorobenzoic acid
Chemical Property:
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:2
  • Exact Mass:232.02080984
  • Heavy Atom Count:16
  • Complexity:336
Purity/Quality:

99.90% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1(=C(C(=C(C(=C1F)F)N=[N+]=[N-])F)N)C(=O)O
Technology Process of 2-Amino-4-azido-3,5,6-trifluorobenzoic acid

There total 5 articles about 2-Amino-4-azido-3,5,6-trifluorobenzoic acid 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 hydroxide; In methanol; water;
DOI:10.1021/jo00298a048
Guidance literature:
Multi-step reaction with 2 steps
1: amberlyst 15 resin / 70 h / Heating
2: NaOH / H2O; methanol / 2 h / 25 °C
With sodium hydroxide; Amberlyst 15 resin; In methanol; water;
DOI:10.1016/S0040-4039(01)80580-3
Guidance literature:
Multi-step reaction with 4 steps
1: 18 percent / H2O2, (n-C4H9)4NHSO4, 20percent aq. NaOH / CH2Cl2 / 40 h / 25 °C
2: 49 percent / NH3 / dimethylsulfoxide / 120 h / 75 °C
3: 88 percent / Amberlyst 15 / 70 h / Heating
4: 98 percent / 20percent aq. NaOH / H2O; methanol
With sodium hydroxide; Amberlyst 15; ammonia; dihydrogen peroxide; tetra(n-butyl)ammonium hydrogensulfate; In methanol; dichloromethane; water; dimethyl sulfoxide;
DOI:10.1021/jo00298a048
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