1,1,1,3,3,3-Hexafluoroisopropyl p-Toluenesulfonate

CAS: 67674-48-0

Ref. 3D-FH60519

Product Information

• Name: 1,1,1,3,3,3-Hexafluoroisopropyl p-Toluenesulfonate
• Synonyms: 1,1,1,3,3,3-Hexafluoroisopropyl Tosylatep-Toluenesulfonic Acid 1,1,1,3,3,3-Hexafluoroisopropyl Ester, 1,1,1,3,3,3-Hexafluoro-2-propyl tosylate, 1,1,1,3,3,3-Hexafluoroisopropyl p-toluenesulphonate, 1,1,1,3,3,3-Hexafluoropropan-2-Yl 4-Methylbenzenesulfonate, 1,1,1,3,3,3-Hexafluoropropan-2-yl 4-methylbenzene-1-sulfonate, 1,1,1,3,3,3-Hexafluoropropan-2-yl p-toluenesulfonate, 2,2,2-Trifluoro-1-(trifluoromethyl)ethyl tosylate, 2-Propanol, 1,1,1,3,3,3-hexafluoro-, 2-(4-methylbenzenesulfonate), 2-Propanol, 1,1,1,3,3,3-hexafluoro-, 4-methylbenzenesulfonate, NSC 179424, p-Toluenesulphonic acid 1,1,1,3,3,3-hexafluoroisopropyl ester
• CAS: 67674-48-0

Description

Hexafluoroisopropanol is a chemical reagent that is used to synthesize esters, amides, and other organic compounds. It is an orthogonal reactant that can be used as both a reagent and catalyst. The product yield of the reaction is determined by the number of equivalents of hexafluoroisopropanol used. Hexafluoroisopropanol is obtained by reacting methylene chloride with p-toluenesulfonyl chloride in the presence of triethylamine. The reaction time can be adjusted by varying the amount of triethylamine in the mixture. Hexafluoroisopropanol reacts with tosylate or chloride to produce esters, amides, chlorides, or sulfonates in a one-pot reaction. The reaction temperature should be kept below room temperature to avoid decomposition and polymerization reactions.

• Brand: Biosynth

Chemical properties

• Molecular weight: 322.23 g/mol
• Formula: C₁₀H₈F₆O₃S
• Purity: Min. 95%
• InChI: InChI=1S/C10H8F6O3S/c1-6-2-4-7(5-3-6)20(17,18)19-8(9(11,12)13)10(14,15)16/h2-5,8H,1H3
• InChI key: InChIKey=QGSVBFAODCJVIZ-UHFFFAOYSA-N
• SMILES: Cc1ccc(S(=O)(=O)OC(C(F)(F)F)C(F)(F)F)cc1