57646-22-7

Basic information

• Product Name: ((2,2,2-trifluoroethoxy)methylene)dibenzene
• Synonyms: ((2,2,2-trifluoroethoxy)methylene)dibenzene
• CAS NO: 57646-22-7
• Molecular Weight: 266.263
• Mol File: 57646-22-7.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: ((2,2,2-trifluoroethoxy)methylene)dibenzene(CAS DataBase Reference)
• NIST Chemistry Reference: ((2,2,2-trifluoroethoxy)methylene)dibenzene(57646-22-7)
• EPA Substance Registry System: ((2,2,2-trifluoroethoxy)methylene)dibenzene(57646-22-7)

Safety Data

• Hazardous Substances Data: 57646-22-7(Hazardous Substances Data)

Upstream product

• 91-01-0 1,1-Diphenylmethanol 
• 1547-96-2 2,4,6-tris(2,2,2-trifluoroethoxy)-1,3,5-triazine 
• 5350-57-2 benzophenone hydrazone 
• 75-89-8 2,2,2-trifluoroethanol 
• 709-82-0 diphenylmethinium 
• 119-61-9 benzophenone 
• 908093-98-1 diazodiphenylmethane 
• 90-99-3 diphenylchloromethane 
• 64-17-5 ethanol 
• 896-65-1 (1,2-diphenylcyclopropyl)benzene 
• 371-67-5 2,2,2-trifluorodiazoethane 

Relevant articles and documents

Proton or Carbene Transfer? On the Dark and Light Reaction of Diazoalkanes with Alcohols

The formal alkylation reaction of OH groups with diazoalkanes under catalyst-free reaction conditions finds broad application in organic synthesis. However, even today, this reaction is mainly limited to the use of diazomethane as reaction partner. In thi

Why are vinyl cations sluggish electrophiles?

The kinetics of the reactions of the vinyl cations 2 [Ph2C=C+-(4-MeO-C6H4)] and 3 [Me2C=C+-(4-MeO-C6H4)] (generated by laser flash photolysis) with diverse nucleophile

Boron Trifluoride?Diethyl Ether-Catalyzed Etherification of Alcohols: A Metal-Free Pathway to Diphenylmethyl Ethers

A novel boron trifluoride?diethyl ether (BF3?OEt2)-catalyzed etherification procedure has been developed in which primary and secondary alcohols are easily converted into diphenylmethyl ethers with yields of up to 99%.