114934-91-7

Basic information

• Product Name: 4-hydroxy-4-(perfluorooctyl)-2,5-cyclohexadien-1-one
• Synonyms: 4-hydroxy-4-(perfluorooctyl)-2,5-cyclohexadien-1-one
• CAS NO: 114934-91-7
• Molecular Weight: 528.165
• Mol File: 114934-91-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-hydroxy-4-(perfluorooctyl)-2,5-cyclohexadien-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4-hydroxy-4-(perfluorooctyl)-2,5-cyclohexadien-1-one(114934-91-7)
• EPA Substance Registry System: 4-hydroxy-4-(perfluorooctyl)-2,5-cyclohexadien-1-one(114934-91-7)

Safety Data

• Hazardous Substances Data: 114934-91-7(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 507-63-1 1-iodoheptadecafluorooctane 
• 106-51-4 p-benzoquinone 

Downstream Products

• 134904-88-4 4-methoxy-4-(perfluorooctyl)-2,5-cyclohexadien-1-one 
• 134904-90-8 ethyl 2-<4-methoxy-4-(perfluorooctyl)-2,5-cyclohexadienylidene>propionate 
• 134904-92-0 ethyl 2-<4-(perfluorooctyl)phenyl>propionate 
• 134904-94-2 2-<4-(perfluorooctyl)phenyl>propionic acid 
• 144876-54-0 2-perfluorooctyl-1,4-benzoquinone 
• 29392-04-9 3-perfluoroocyl-1,4-dihydroxybenzene 
• 134641-35-3 4-heptadecafluorooctylbenzaldehyde 
• 135957-84-5 1,4-Bis(perfluorooctyl)-2,5-cyclohexadiene-1,4-diol 
• 134285-00-0 4-Perfluorooctyl-1,2-benzenediol 
• 134284-96-1 4-Perfluorooctyl-1,3-benzenediol 
• 114963-31-4 1,2-Diacetoxy-4-perfluorooctylbenzene 
• 114963-34-7 2,4-Diacetoxy-1-perfluorooctylbenzene 
• 114963-28-9 4-Acetoxy-4-perfluorooctyl-2,5-cyclohexadien-1-one 
• 135957-91-4 2,5-Dimethyl-5-perfluorooctyl-2-cyclohexene-1,4-dione 

Relevant articles and documents

Acetic acid derivatives and their production

Compounds of formula STR1 where n is an integer from 1 to 12, R and R1 are the same or different and are hydrogen or C1 to C6 linear or branched alkyl as well as their physiologically active salts and amides thereof and the enantiomers, mixtures and racemates are disclosed. Intermediates useful in preparing the above compounds are also disclosed as are processes for preparing these compounds.

Synthesis of 2-[(perfluoroalkyl)phenyl]propionic acids

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Perfluoralkyl-thwarted Rearrangement of Quinol Esters. Formation of Catechol Derivatives via 1,3-Migration of Acyloxyl Group

Treatment of 4-perfluoroalkyl-4-quinols with acetic anhydride-sulfuric acid was found to lead to 1,2- and 1,3-migration of acetoxyl group in initially formed quinol acetates followed by aromatization to give a mixture of 4-perfluoroalkylresorcinol diaceta