2010-61-9

Usage

Uses

Used in Adhesive Industry:
HEXAFLUORO-2-(P-TOLYL)ISOPROPANOL is used as a key component in the production of polyurethane adhesive resin compounds containing rubber particles. Its incorporation enhances the adhesive properties, making it suitable for various bonding applications.
Used in Mobile Device Manufacturing:
In the mobile device industry, HEXAFLUORO-2-(P-TOLYL)ISOPROPANOL is utilized in the production of polyurethane resin compounds and adhesive tapes. Its use in this sector is attributed to its ability to improve the durability and performance of the adhesives, ensuring a strong bond between components and contributing to the overall quality of the devices.

InChI:InChI=1/C10H8F6O/c1-6-2-4-7(5-3-6)8(17,9(11,12)13)10(14,15)16/h2-5,17H,1H3

Upstream product

• 684-16-2 Hexafluoroacetone 
• 108-88-3 toluene 
• 106-38-7 para-bromotoluene 

Downstream Products

• 2396-26-1 1-methyl-4-(perfluoropropan-2-yl)benzene 
• 30129-13-6 Hexafluordihydro-α-terpineol 
• 101980-06-7 1-(p-tolyl)-1-(trifluoromethyl)-2,2,2-trifluoroethyl tosylate 
• 16261-80-6 4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]benzoic acid 
• 202134-57-4 2-(4-(bromomethyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol 
• 101980-19-2 1-Methyl-4-[2,2,2-trifluoro-1-(2,2,2-trifluoro-ethoxy)-1-trifluoromethyl-ethyl]-benzene 
• 101980-16-9 Trifluoro-acetic acid 2,2,2-trifluoro-1-p-tolyl-1-trifluoromethyl-ethyl ester 
• 88911-72-2 C₁₀H₆F₆N₂O₅ 
• 35445-56-8 p-Methyl-3-nitro-hexafluorcuminol 

Relevant academic research and scientific papers

Design and synthesis of chiral oxathiozinone scaffolds: Efficient synthesis of hindered enantiopure sulfinamides and sulfinyl ketimines

Is that S-O? The title scaffolds have a highly active and properly differentiated S-O bond for the efficient synthesis of enantiopure sulfinamides. The method is practical, green, and has the potential to provide an economical commercial process for the synthesis of bulky sulfinamides. Copyright

Doubly Destabilized Carbocations. Strong Aryl Delocalization and the Attenuation of Rate Decelerating Effects of CF3 and CN Groups

Solvolysis rates of ArC(CF3)2OTs in CF3CO2H give an excellent correlation log k = -10.7?+-8.69, and a point for the p-Me2N compound derived from the rate of the p-nitrobenzoate also fits this correlation, giving a span of 1E19 in reactivity.Limiting values of ρ+ of -10 to -12 for generation of benzylic cations in the gas phase and solution have been reached.Rate ratios k(ArCH(OTs)CF3)/k(ArC(CF3)2OTs) increase from 2.4 to 54 with decreasing aryl donor power; these k(H)/k(CF3) ratios are much less than typical values of 1E6 in more stabilized systems.Displacement of the p-MeO group occurs in solvolysis of p-MeOC6H4C(CF3)2OTs (9) in EtOH and CD3OH.Trifluoroacetolysis of ArC(OTs)(CF3)CN (Ar = p-Tol (13) and Ph) gives ρ+ = -12.1, and for 13 in different solvents the reactivity is greater than p-TolCH(OTs)CF3 by factors of 8.6 to 175.This is the first observation of k(CN)/k(H) ratios greater than 1.0.All these results, plus the rather modest dependence of the rates on solvent polarity (m = 0.76 for 9 and 0.66 for 13), are interpreted in terms of carbocationic transition states and intermediates in which the charge is largely delocalized onto the aryl group.