130755-51-0

Basic information

• Product Name: 5-amino-4-bromochlorofluoromethylthio-3-cyano-1-(2,4,6-trichlorophenyl)-1H-pyrazole
• CAS NO: 130755-51-0
• Molecular Weight: 464.96
• Mol File: 130755-51-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-amino-4-bromochlorofluoromethylthio-3-cyano-1-(2,4,6-trichlorophenyl)-1H-pyrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-amino-4-bromochlorofluoromethylthio-3-cyano-1-(2,4,6-trichlorophenyl)-1H-pyrazole(130755-51-0)
• EPA Substance Registry System: 5-amino-4-bromochlorofluoromethylthio-3-cyano-1-(2,4,6-trichlorophenyl)-1H-pyrazole(130755-51-0)

Safety Data

• Hazardous Substances Data: 130755-51-0(Hazardous Substances Data)

Upstream product

• 353-55-9 dibromochlorofluoromethane 
• 130755-50-9 4,4'-dithiobis[5-amino-3-cyano-1(2,4,6-trichlorophenyl)-1H-pyrazole] 

Relevant articles and documents

Reactions of Bromotrifluoromethane and Related Halides. Part 12. Transformation of Disulfides into Perfluoroalkyl Sulfides in the Presence of Sulfoxylate Anion Radical Precursors

Perfluoroalkyl sulfides are prepared by reaction of perfluoroalkyl halides with disulfides in the presence of sulfoxylate anion radical precursors.Aliphatic, aromatic and heteroaromatic disulfides bearing cyano, ester and amino functional groups have been employed; a variety of perhalogenoalkanes can also be employed, e.g.CF3(CF2)nI, CF3Br, CF2Br2, CF2BrCl, CFCl3 and CF2ClCFCl2.The most convenient sulfoxylate anion radical precursor for this reaction is formed by a combination of sodium formate and sulfur dioxide.