78522-69-7

Basic information

• Product Name: 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl trifluoromethanesulfonate
• Synonyms: 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl trifluoromethanesulfonate
• CAS NO: 78522-69-7
• Molecular Weight: 496.169
• Mol File: 78522-69-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl trifluoromethanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl trifluoromethanesulfonate(78522-69-7)
• EPA Substance Registry System: 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl trifluoromethanesulfonate(78522-69-7)

Safety Data

• Hazardous Substances Data: 78522-69-7(Hazardous Substances Data)

Upstream product

• 358-23-6 trifluoromethylsulfonic anhydride 
• 647-42-7 1H,1H,2H,2H-tridecafluoro-n-octanol 
• 1493-13-6 trifluorormethanesulfonic acid 
• 2043-57-4 1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane 

Downstream Products

• 647-42-7 1H,1H,2H,2H-tridecafluoro-n-octanol 
• 25291-17-2 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene 
• 78522-74-4 1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyloxy)-octane 
• 512169-13-0 O-benzyl-N-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)hydroxylamine 
• 1643531-04-7 C₃₄H₂₆F₁₃NO₈S 
• 1643531-10-5 C₄₄H₄₉F₁₃N₄O₁₀S₂ 
• 1643530-99-7 C₃₂H₂₂F₁₃NO₅ 
• 1643531-22-9 C₃₇H₃₄F₁₃N₂O₅⁽¹⁺⁾ 
• 512169-29-8 N-benzyloxy-2-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-undecyloxy)-N-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyl)-acetamide 
• 512169-18-5 N-benzyloxy-2,2,3,3,4,4,4-heptafluoro-N-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyl)-butyramide 
• 512169-16-3 octanoic acid benzyloxy-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyl)-amide 
• 512169-27-6 N-benzyloxy-2-(4-chloro-butoxy)-N-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyl)-acetamide 
• 512169-35-6 N-benzyloxy-2-(2-ethoxy-ethoxy)-N-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyl)-acetamide 
• 512169-24-3 N-benzyloxy-2-pentyloxy-N-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyl)-acetamide 

Relevant articles and documents

Surface modification by electrostatic self-assembly followed by covalent fixation

Sticks and bonds: Surface-modifying agents can be functionalized with ionic groups that enable high exhaustion from a processing bath through electrostatic self-assembly. Using cyclic oniums as the ionic functional groups, thermally induced ring-opening converts the ionic bonds to covalent bonds, thus lending permanency to the modification of the surface.

Preparation of bis(polyfluoroalkyl)cyclopentadienes, new highly fluorophilic ligands for fluorous biphase catalysis

Bis[2-(perfluoroalkyl)ethyl]cyclopentadienes were synthesized from lithium [2-(perfluoroalkyl)ethyl]cyclopentadienides and 2-(perfluoroalkyl)ethyl triflates as mixtures of four regioisomers, structure of which was determined by 1H and 13/

2-(perfluoroalkyl)ethyl triflates, building blocks for the synthesis of bis(polyfluoroalkylated) cyclopentadienes

Fluorinated building blocks, 2-(perfluorohexyl)ethyl triflate (11a) and 2-(perfluorooctyl)ethyl triflate (11b) were prepared from the corresponding fluoroalkanols and triflic anhydride. Fluorinated triflates 11 were employed for the preparation of bis(pol