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Benzene, 1,1',1''-methylidynetris[2,3,4,5,6-pentafluoro- is a complex organic compound with the chemical formula C18H3F15. It is a derivative of benzene, where three 2,3,4,5,6-pentafluorobenzene units are connected through a central methylidyne bridge. Benzene, 1,1',1''-methylidynetris[2,3,4,5,6-pentafluoro- is characterized by its highly fluorinated nature, which imparts unique chemical and physical properties. It is often used in the synthesis of various fluorinated compounds and materials, such as specialty polymers and pharmaceuticals, due to its stability and reactivity. The compound's structure and properties make it a valuable intermediate in organic synthesis and a component in advanced materials science.

4780-60-3

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4780-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4780-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,8 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4780-60:
(6*4)+(5*7)+(4*8)+(3*0)+(2*6)+(1*0)=103
103 % 10 = 3
So 4780-60-3 is a valid CAS Registry Number.

4780-60-3Relevant academic research and scientific papers

Revisiting the Perfluorinated Trityl Cation

Delany, Eoghan G.,Kaur, Satnam,Cummings, Steven,Basse, Kristoffer,Wilson, David J. D.,Dutton, Jason L.

supporting information, p. 5298 - 5302 (2019/03/11)

Although ultimately not isolable for X-ray structural characterization, the free perfluorinated trityl cation was shown to be observable in neat triflic acid, which represents milder conditions than previous reports of this cation in “magic acid” or oleum. A triflate-bound species could be generated in organic solvents using stoichiometric amounts of triflic acid and was shown to be synthetically viable for hydride abstraction from Et3SiH. It was demonstrated that the para-position on the -C6F5 rings is the primary point of attack for decomposition of the cation.

Fluorocarbanion chemistry. Tris(4-nitro-2,3,5,6-tetrafluorophenyl) methane and companions

Filler, Robert,Fiebig Jr., August E.,Mandal, Braja K.

, p. 185 - 188 (2007/10/03)

The titled compound (2) is prepared by oxidation of tris(4-amino-2,3,5,6-tetrafluorophenyl) methane with 98% H2O2 and trifluoroacetic anhydride. Compound 2, a strong carbon acid, forms long-persisting deep blue solutions of the anion

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