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sodium 2-fluorobenzenesulfinate

Base Information
  • Chemical Name:sodium 2-fluorobenzenesulfinate
  • CAS No.:127159-66-4
  • Molecular Formula:C6H4FO2S*Na
  • Molecular Weight:182.151
  • Hs Code.:
sodium 2-fluorobenzenesulfinate

Synonyms:sodium 2-fluorobenzenesulfinate

Suppliers and Price of sodium 2-fluorobenzenesulfinate
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
  • American Custom Chemicals Corporation
  • 2-FLUOROBENZENESULFINIC ACID SODIUM SALT 95.00%
  • 5MG
  • $ 496.05
  • AK Scientific
  • Sodium2-fluorobenzenesulfinate
  • 10g
  • $ 1918.00
  • AK Scientific
  • Sodium2-fluorobenzenesulfinate
  • 1g
  • $ 522.00
  • AK Scientific
  • Sodium2-fluorobenzenesulfinate
  • 100mg
  • $ 210.00
Total 3 raw suppliers
Chemical Property of sodium 2-fluorobenzenesulfinate
Chemical Property:
Purity/Quality:

98%Min *data from raw suppliers

2-FLUOROBENZENESULFINIC ACID SODIUM SALT 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of sodium 2-fluorobenzenesulfinate

There total 2 articles about sodium 2-fluorobenzenesulfinate 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 carbonate; sodium sulfite; In water; at 50 ℃; for 2h;
DOI:10.1016/j.tetlet.2014.04.111
Guidance literature:
With tris(dibenzylideneacetone)dipalladium(0) chloroform complex; 1,2-bis-(diphenylphosphino)ethane; In 1,2-dichloro-ethane; at 50 ℃; for 12h; stereoselective reaction;
DOI:10.1002/cctc.201901292
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