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1-Fluoro-2,4,6-trinitrobenzene

Base Information Edit
  • Chemical Name:1-Fluoro-2,4,6-trinitrobenzene
  • CAS No.:364-44-3
  • Molecular Formula:C6H2 F N3 O6
  • Molecular Weight:231.097
  • Hs Code.:2904909090
  • European Community (EC) Number:206-661-3
  • NSC Number:137771
  • DSSTox Substance ID:DTXSID9074806
  • Nikkaji Number:J193.867C
  • Wikidata:Q82002978
  • Mol file:364-44-3.mol
1-Fluoro-2,4,6-trinitrobenzene

Synonyms:trinitrofluorobenzene

Suppliers and Price of 1-Fluoro-2,4,6-trinitrobenzene
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
  • American Custom Chemicals Corporation
  • 2,4,6-TRINITROFLUOROBENZENE 95.00%
  • 5MG
  • $ 501.41
Total 9 raw suppliers
Chemical Property of 1-Fluoro-2,4,6-trinitrobenzene Edit
Chemical Property:
  • Vapor Pressure:6.36E-05mmHg at 25°C 
  • Boiling Point:355.5°Cat760mmHg 
  • Flash Point:168.8°C 
  • PSA:137.46000 
  • Density:1.789g/cm3 
  • LogP:3.11990 
  • XLogP3:0.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:0
  • Exact Mass:230.99276295
  • Heavy Atom Count:16
  • Complexity:296
Purity/Quality:

99%, *data from raw suppliers

2,4,6-TRINITROFLUOROBENZENE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=C(C=C(C(=C1[N+](=O)[O-])F)[N+](=O)[O-])[N+](=O)[O-]
Technology Process of 1-Fluoro-2,4,6-trinitrobenzene

There total 5 articles about 1-Fluoro-2,4,6-trinitrobenzene 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 fuming sulphuric acid; potassium nitrate; at 0 - 125 ℃; for 120h;
DOI:10.1021/acs.cgd.0c01049
Guidance literature:
With diethylamino-sulfur trifluoride;
DOI:10.1002/(SICI)1099-1395(199608)9:8<515::AID-POC816>3.0.CO;2-5
Guidance literature:
With potassium fluoride; at 185 ℃; for 5h;
Refernces Edit
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