247018-51-5

Basic information

• Product Name: 4-t-butylphenyl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
• Synonyms: 4-t-butylphenyl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
• CAS NO: 247018-51-5
• Molecular Weight: 432.307
• Mol File: 247018-51-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-t-butylphenyl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-t-butylphenyl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate(247018-51-5)
• EPA Substance Registry System: 4-t-butylphenyl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate(247018-51-5)

Safety Data

• Hazardous Substances Data: 247018-51-5(Hazardous Substances Data)

Upstream product

• 98-54-4 para-tert-butylphenol 
• 32848-23-0 para-nitrophenyl perfluorobutanesulfonate 
• 375-72-4 Nonafluorobutanesulfonyl fluoride 

Downstream Products

• 255835-92-8 (4-tert-butylphenyl)(4-methoxyphenyl)amine 
• 4496-49-5 4-tert-butyldiphenylamine 
• 898082-19-4 4-(tert-butyl)-N-morpholinobenzenesulfonamide 
• 208188-23-2 N-methoxy-N-methyl-4-(2-methyl-2-propanyl)benzamide 
• 1448632-01-6 (4-(tert-butyl)phenyl)diphenylphosphine oxide 
• 1435392-63-4 5-(4-tert-butylbenzyl)-dihydrofuran-2(3H)-one 
• 253185-03-4 tert-butylbenzene 
• 98-54-4 para-tert-butylphenol 
• 1459122-86-1 1-(tert-butyl)-4-(2,2,2-trifluoroethoxy)benzene 
• 1625-92-9 4-tert-butylbiphenyl 
• 5396-38-3 1-(tert-butyl)-4-methoxybenzene 
• 20330-45-4 4-tert-butylacetanilide 
• 222723-04-8 N-(4-tert-butylphenyl)-N-phenylacetamide 
• 1198293-96-7 benzyl butyl(4-tert-butylphenyl)carbamate 

Relevant articles and documents

Palladium-Catalyzed C-P Bond-Forming Reactions of Aryl Nonaflates Accelerated by Iodide

An iodide-accelerated, palladium-catalyzed C-P bond-forming reaction of aryl nonaflates is described. The protocol was optimized for the synthesis of aryl phosphine oxides and was found to be tolerant of a wide range of aryl nonaflates. The general nature of this transformation was established with coupling to other P(O)H compounds for the synthesis of aryl phosphonates and an aryl phosphinate. The straightforward synthesis of stable, isolable aryl nonaflates, in combination with the rapid C-P bond-forming reaction allows facile preparation of aryl phosphorus target compounds from readily available phenol starting materials. The synthetic utility of this general strategy was demonstrated with the efficient preparation of an organic light-emitting diode (OLED) material and a phosphonophenylalanine mimic.

A high throughput synthesis of aryl triflate and aryl nonaflate promoted by a polymer supported base (PTBD)

A rapid synthesis of aryl triflate and aryl nonaflate was developed using 4-nitrophenyl triflate and 4-nitrophenyl nonaflate as perfluoroalkanesulfonyl transfer reagents in combination with a polymer supported base (PTBD). Simple filtration of the reactio