967-95-3

Usage

Uses

Used in Organic Chemistry:
4-(4-Dimethylaminophenyl)-2-(4-dipropylaminophenyl)-5-(2-fluorophenyl)oxazole is used as a reagent and intermediate for the synthesis of various pharmaceutical compounds and biologically active molecules. Its distinct chemical properties and potential biological activities, attributed to its substituent groups, make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(4-Dimethylaminophenyl)-2-(4-dipropylaminophenyl)-5-(2-fluorophenyl)oxazole is utilized as a key component in the development of new drugs. Its unique structure and functional groups allow for the creation of molecules with specific biological activities, potentially leading to the discovery of novel therapeutic agents for various medical conditions.

Upstream product

• 16853-85-3 lithium aluminium tetrahydride 
• 1043-50-1 pentafluorophenyl sulfide 
• 769-40-4 2,3,5,6-tetrafluorothiophenol 
• 1535-95-1 2,2',3,3',5,5',6,6'-octafluorodiphenyl disulfide 
• 973-17-1 bis(pentafluorophenyl)mercury(II) 
• 1927-90-8 pentafluorophenyl-2,3,5,6-tetrafluorophenylsulfane 
• 1927-89-5 4,4'-bis(pentafluorophenylmercapto)-octafluorobiphenyl 
• 973-18-2 bis(perfluorophenyl) selenide 
• 1835-58-1 4-bromotetrafluorophenyl(pentafluorophenyl)sulfane 
• 1835-57-0 2,3,5,6-tetrafluoro-1,4-bis(pentafluorophenylsulfanyl)benzene 
• 36650-02-9 trifluoro(pentafluorophenyl)sulfur(IV) 
• 879-05-0 2,3,4,5,6-pentafluorophenylmagnesium bromide 
• 1076-44-4 pentafluorophenyl lithium 
• 10386-84-2 4,4'-dibromo-2,3,5,6,2',3',5',6'-octafluoro-1,1'-biphenyl 

Downstream Products

• 56354-51-9 C₂₄F₁₈S₃ 

Relevant academic research and scientific papers

Convenient Synthesis of Symmetrical Polyfluorinated Diphenyl Sulfides

Abstract: Thermal properties of decafluorodiphenyl disulfide in the pure state and in the presence of copper and iron metals have been studied. A procedure has been proposed for the synthesis of symmetrical poly-fluorinated diaryl sulfides from diaryl dis

REACTION OF PERFLUOROARYL HALIDES WITH REDUCED SPECIES OF SULFUR DIOXIDE (HSO2(-), SO2(2-), S2O4(2-))

Rongalite (sodium hydroxymethanesulfinate), sodium dithionite, and aminoiminomethanesulfinic acid (AIMS) reduce perfluoroiodobenzene in N,N-dimethylformamide to pentafluorobenzene.In the presence of added D2O or CH3OD, deuteriopentafluorobenzene is formed. p-Dinitrobenzene does not inhibit the reduction, and addition of norbonene did not result in trapping of any radical intermediates.Reaction of pentafluoroiodobenzene with sodium benzenesulfinate gave 1,4-dibenzenesulfonyl-2,3,5,6-tetrafluorobenzene.A halophilic attack mechanism is suggested for the reduction reaction.Chloropentafluorobenzene did not react under the same conditions as the iodide; at elevated temperatures in the presence of sodium bicarbonate and Rongalite the fluorine para to the chlorine was reduced.Reduction of the chloride to pentafluorobenzene is minor.In the absence of bicarbonate, the chloride gave also a mixture of sulfides believed to be derived from decomposition of the Rongalite to hydrogen sulfide.Some reaction with dimethylamine from decomposition of DMF also is observed.