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2-Nitrophenyl trifluoromethyl sulfide

Base Information Edit
  • Chemical Name:2-Nitrophenyl trifluoromethyl sulfide
  • CAS No.:1644-87-7
  • Molecular Formula:C7H4F3NO2S
  • Molecular Weight:223.175
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10431189
  • Nikkaji Number:J1.333.808F
  • Wikidata:Q82245010
  • Mol file:1644-87-7.mol
2-Nitrophenyl trifluoromethyl sulfide

Synonyms:2-nitrophenyl trifluoromethyl sulfide;1644-87-7;SCHEMBL7007001;DTXSID10431189;2- (Trifluoromethylthio)nitrobenzene;MFCD22054900;1-(Trifluoromethylthio)-2-nitrobenzene

Suppliers and Price of 2-Nitrophenyl trifluoromethyl sulfide
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 2-Nitrophenyl trifluoromethyl sulfide Edit
Chemical Property:
  • XLogP3:3.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:1
  • Exact Mass:222.99148403
  • Heavy Atom Count:14
  • Complexity:216
Purity/Quality:

98%min *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C(=C1)[N+](=O)[O-])SC(F)(F)F
Technology Process of 2-Nitrophenyl trifluoromethyl sulfide

There total 19 articles about 2-Nitrophenyl trifluoromethyl sulfide 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 various solvent(s); at 150 ℃; for 5h; on alumina support;
DOI:10.1016/S0022-1139(00)80437-6
Guidance literature:
With copper(l) iodide; potassium carbonate; In acetonitrile; at 20 ℃; for 12h;
DOI:10.1016/j.tetlet.2019.04.018
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