51740-38-6

Basic information

• Product Name: 1-Octanol, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-, 4-methylbenzenesulfonate
• CAS NO: 51740-38-6
• Molecular Formula: C15H11F13O3S
• Molecular Weight: 518.296
• Mol File: 51740-38-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1-Octanol, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-, 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Octanol, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-, 4-methylbenzenesulfonate(51740-38-6)
• EPA Substance Registry System: 1-Octanol, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-, 4-methylbenzenesulfonate(51740-38-6)

Safety Data

• Hazardous Substances Data: 51740-38-6(Hazardous Substances Data)

Upstream product

• 647-42-7 1H,1H,2H,2H-tridecafluoro-n-octanol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 34451-26-8 2-perfluorohexylethanethiol 
• 1616596-38-3 N-(2-hydroxyethyl)-N,N-dimethyl-3,3,4,4,5,5,6,6,7,7,8,8,8-tride-cafluorooctane-1-ammonium tosylate 
• 1224408-59-6 C₁₆H₁₀F₁₃N₃ 

Relevant articles and documents

Macrocyclic ligands with partially fluorinated sidearms: Synthesis and metal ion complexation

Derivatives of aza-12-crown-4, aza-15-crown-5, aza-18-crown-6, 1,10- diaza-18-crown-6 and 1,4,8,12-tetraazacyclopentadecane with partially fluorinated substituents attached to nitrogen are prepared. Their efficiencies and selectivities in alkali metal and

Methods for Making Functionalized Fluorinated Monomers, Fluorinated Monomers, and Compositions for Making the Same

A method of making a functionalized fluorinated monomer for use in making oligomers and polymers that can be used to improve surface properties of polymer-derived systems, such as coatings. The method of making a functionalized fluorinated monomer includes reacting at least one fluorinated nucleophilic reactant, such as a fluorinated alcohol, with at least one compound containing at least one epoxide group. Other methods include reaction of a fluorinated alcohol with a cyclic carboxylic anhydride. In another embodiment, a method includes reacting a fluorinated mesylate, tosylate or triflate with an amine, alkoxide or phenoxide. In other embodiments, the method includes reacting a fluorinated alcohol with an alkyl halide, or reacting a fluorinated alkyl halide with an amine. The functionalized fluorinated monomers may be used as intermediates and reacted to modify the functional groups thereon. Further, the functionalized fluorinated monomers may be reacted to form polymers or oligomers, or with polymers or oligomers having functional groups to modify the polymer or oligomer through the functional group thereon,

Novel fluorinated dialkylphosphonatocholines: Synthesis, physicochemical properties and antiprotozoal activities against Acanthamoeba spp.

The synthesis of four new organophosphorous gemini surfactants is presented. They belong to the class of dialkylphosphonatocholines. Tails are represented with two octyl groups both non or partially fluorinated. The synthesis was performed by reaction of alkylphosphonic acids with choline derivatives in the presence of 2,4,6-triisopropylbenzenesulfonyl chloride. The micellar, surface active, and solubilization properties of new surfactants were studied. Antiprotozoal activities were tested against Acanthamoeba lugdunensis and Acanthamoeba quina.