33288-22-1

Basic information

• Product Name: C₆F₅S(n-C₄H₉)
• Synonyms: C₆F₅S(n-C₄H₉)
• CAS NO: 33288-22-1
• Molecular Weight: 256.239
• Mol File: 33288-22-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₆F₅S(n-C₄H₉)(CAS DataBase Reference)
• NIST Chemistry Reference: C₆F₅S(n-C₄H₉)(33288-22-1)
• EPA Substance Registry System: C₆F₅S(n-C₄H₉)(33288-22-1)

Safety Data

• Hazardous Substances Data: 33288-22-1(Hazardous Substances Data)

Upstream product

• 542-69-8 1-iodo-butane 
• 771-62-0 pentafluorophenylthiol 
• 5184-59-8 S-butyl benzenesulfonothioate 
• 1206-46-8 trimethyl(pentafluorophenyl)silane 
• 51098-05-6 Methyl-dithiocarbamic acid pentafluorophenyl ester 
• 344-07-0 1-chloro-2,3,4,5,6-pentafluorobenzene 
• 27918-31-6 pentafluorobenzenesulfenyl chloride 
• 106-98-9 1-butylene 
• 344-04-7 bromopentafluorobenzene 
• 4860-18-8 Copper(I) n-butanethiolate 
• 879-05-0 2,3,4,5,6-pentafluorophenylmagnesium bromide 
• 1076-44-4 pentafluorophenyl lithium 
• 392-56-3 Hexafluorobenzene 
• 106-97-8 n-butane 

Downstream Products

• 2266-69-5 n-Dodecanoyl fluoride 
• 1336931-36-2 1-n-butylthio-4-(4-cyanophenoxy)-2,3,5,6-tetrafluorobenzene 
• 1251445-50-7 3,5-dimethoxybenzoyl fluoride 
• 1336931-52-2 4-butylthio-2,3,5,6-tetrafluorophenyl 4-tolyl sulfide 
• 35779-12-5 (butylsulfonyl)pentafluorobenzene 

Relevant articles and documents

The organocatalytic synthesis of perfluorophenylsulfides: Via the thiolation of trimethyl(perfluorophenyl)silanes and thiosulfonates

The organic superbase t-Bu-P4-catalyzed direct thiolation of trimethyl(perfluorophenyl)silanes and thiosulfonates was developed. Yields of perfluorophenylsulfides of up to 97% under catalysis of 5 mol% t-Bu-P4 were achieved. This method was shown to provide an efficient way to construct the perfluorophenyl-sulfur bond under mild metal-free reaction conditions. This journal is