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Perfluoro-(1,1':4',1'':4'',1''':4''',1''''-quinquephenyl) is a complex organic compound consisting of a quinquephenyl core, which is a pentameric (five-ring) structure made up of five benzene rings. Each benzene ring in the molecule is fully fluorinated, meaning that all hydrogen atoms are replaced by fluorine atoms. This results in a highly stable and chemically inert molecule with unique properties, such as high thermal and oxidative stability, low surface energy, and excellent resistance to chemical degradation. Due to these characteristics, perfluoro-quinquephenyl and its derivatives have potential applications in various fields, including materials science, electronics, and as components in specialty coatings or lubricants. However, the synthesis and handling of such highly fluorinated compounds can be challenging, and their environmental impact and potential health risks should be carefully considered.

5630-57-9

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5630-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5630-57-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5630-57:
(6*5)+(5*6)+(4*3)+(3*0)+(2*5)+(1*7)=89
89 % 10 = 9
So 5630-57-9 is a valid CAS Registry Number.

5630-57-9Downstream Products

5630-57-9Relevant academic research and scientific papers

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

Nishida, Masakazu,Hayakawa, Yoshio,Ono, Taizo

experimental part, p. 1314 - 1321 (2011/02/22)

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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