203255-90-7

Basic information

• Product Name: Peroxide, bis[(undecafluorocyclohexyl)carbonyl]
• Synonyms: bis-perfluorocyclohexanoylperoxide
• CAS NO: 203255-90-7
• Molecular Formula: C14F22O4
• Molecular Weight: 650.116
• Mol File: 203255-90-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Peroxide, bis[(undecafluorocyclohexyl)carbonyl](CAS DataBase Reference)
• NIST Chemistry Reference: Peroxide, bis[(undecafluorocyclohexyl)carbonyl](203255-90-7)
• EPA Substance Registry System: Peroxide, bis[(undecafluorocyclohexyl)carbonyl](203255-90-7)

Safety Data

• Hazardous Substances Data: 203255-90-7(Hazardous Substances Data)

Upstream product

• 6588-63-2 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexanecarbonyl fluoride 

Downstream Products

• 124-38-9 carbon dioxide 
• 24517-89-3 Perfluorcyclohexyl 

Relevant articles and documents

Novel perfluorocyclohexylation with bis(perfluorocyclohexane carbonyl) peroxide

A new bis(perfluorocyclohexane carbonyl) peroxide was prepared by the reaction of the corresponding acyl fluoride and hydrogen peroxide. This peroxide was applicable for the direct introduction of perfluorocyclohexyl group into various organic molecules such as acrylic acid oligomer, benzene and polystyrene; in particular interest, not only equatorial but also axial conformational isomers were isolated in phenylperfluorocyclohexane thus obtained.

Novel perfluoroalkyl vinyl ether compound, process for preparing copolymer by using the compound, and optical plastic materials comprising copolymer prepared by the process

Disclosed herein are a novel perfluoroalkyl vinyl ether compound, a process for preparing a copolymer by using the perfluoroalkyl vinyl ether compound, and an optical plastic material comprising a copolymer prepared by the process. More specifically, the perfluoroalkyl vinyl ether has a particular molecular structure; the process is performed by copolymerizing the perfluoroalkyl vinyl ether compound with a common fluorinated olefin in the presence of a perfluorinated radical initiator; and, the optical plastic material comprises a copolymer prepared by the process and optionally a dopant. The copolymerization of the perfluoroalkyl vinyl ether with a common fluorinated olefin can provide a copolymer having a high molecular weight. In addition, appropriate control of the composition of the monomers can provide a completely amorphous copolymer. Since the polymer prepared by the process exhibits excellent thermal properties and is substantially transparent in the UV and near IR regions, it can be usefully applied to various optical plastic materials. Furthermore, a preform for a GI type plastic optical fiber fabricated by using the copolymer and the dopant has a high Tg, thus being stable, and a parabolic refractive index profile due to the presence of the dopant.