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4-pentafluorophenyl 4'-trifluoromethyl perfluoro biphenyl is a complex organic compound characterized by its highly fluorinated structure. It consists of two phenyl rings, each containing six carbon atoms, with one of the rings having four fluorine atoms and the other having three fluorine atoms, in addition to a trifluoromethyl group attached to the latter. 4-pentafluorophenyl 4`-trifluoromethyl perfluoro biphenyl is known for its unique electronic properties and chemical stability due to the presence of fluorine atoms, which confer resistance to many chemical reactions. It is often used in specialized applications such as in the production of high-performance materials and as a component in certain types of chemical research. The compound's specific structure and properties make it a subject of interest in fields where thermal and chemical stability are paramount.

5492-87-5

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5492-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5492-87-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,9 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5492-87:
(6*5)+(5*4)+(4*9)+(3*2)+(2*8)+(1*7)=115
115 % 10 = 5
So 5492-87-5 is a valid CAS Registry Number.

5492-87-5Downstream Products

5492-87-5Relevant academic research and scientific papers

Formation of perfluorinated polyphenylenes by multiple pentafluorophenylation using C6F5Si(CH3) 3

Nishida, Masakazu,Hayakawa, Yoshio,Ono, Taizo

, p. 1314 - 1321 (2010)

Pentafluorophenylation of perfluoroarenes with C6F 5Si(CH3)3 was investigated by using NMR and MALDI-TOF-MS techniques. Successive multiple pentafluorophenylation easily occurred not only on the para-position but also on the ortho-positions to provide perfluorinated p-phenylene and m-phenylene compounds. The perfluoroarenes having electron-withdrawing substituents provided oligo- to poly-(phenylene)s depending on the added amounts of C6F 5Si(CH3)3, while the perfluoroarenes having electron-donor substituents gave H(C6F4)nF polymers produced from C6F5H, which was the decomposed product of C6F5Si(CH3)3.

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