117482-26-5

Basic information

• Product Name: Phosphoric acid diethyl ester (E)-2,3,3,3-tetrafluoro-1-phenyl-propenyl ester
• Synonyms: Phosphoric acid diethyl ester (E)-2,3,3,3-tetrafluoro-1-phenyl-propenyl ester
• CAS NO: 117482-26-5
• Molecular Weight: 342.227
• Mol File: 117482-26-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Phosphoric acid diethyl ester (E)-2,3,3,3-tetrafluoro-1-phenyl-propenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphoric acid diethyl ester (E)-2,3,3,3-tetrafluoro-1-phenyl-propenyl ester(117482-26-5)
• EPA Substance Registry System: Phosphoric acid diethyl ester (E)-2,3,3,3-tetrafluoro-1-phenyl-propenyl ester(117482-26-5)

Safety Data

• Hazardous Substances Data: 117482-26-5(Hazardous Substances Data)

Upstream product

• 394-52-5 pentafluoroethyl phenyl ketone 
• 2303-76-6 sodium diethyl phosphite 

Downstream Products

• 2267-65-4 phenyl 1,2,2,2,-tetrafluoroethyl ketone 
• 126255-60-5 2-fluoro-1-phenyl-2-(trifluoromethyl)-1,3-hexanediol 
• 126255-60-5 1,2-syn-2,3-syn-2-fluoro-1-phenyl-2-(trifluoromethyl)-1,3-hexanediol 
• 126255-61-6 2-fluoro-1,3-diphenyl-2-(trifluoromethyl)-1,3-propanediol 
• 126255-61-6 2-fluoro-1,3-diphenyl-2-(trifluoromethyl)-1,3-propanediol 
• 126255-62-7 5-fluoro-2,2-dimethyl-4-phenyl-6-propyl-5-(trifluoromethyl)-1,3-dioxane 
• 126255-62-7 5-fluoro-2,2-dimethyl-4-phenyl-6-propyl-5-(trifluoromethyl)-1,3-dioxane 
• 126255-63-8 5-fluoro-2,2-dimethyl-4,6-diphenyl-5-(trifluoromethyl)-1,3-dioxane 
• 126255-64-9 5-fluoro-2,2-dimethyl-4,6-diphenyl-5-(trifluoromethyl)-1,3-dioxane 
• 125741-97-1 2-Fluoro-3-hydroxy-1-phenyl-2-trifluoromethyl-hexan-1-one 
• 125741-97-1 2-fluoro-3-hydroxy-1-phenyl-2-(trifluoromethyl)-1-hexanone 
• 125741-97-1 2-fluoro-3-hydroxy-1-phenyl-2-(trifluoromethyl)-1-hexanone 
• 125741-99-3 2,3,3,3-Tetrafluoro-2-(hydroxy-phenyl-methyl)-1-phenyl-propan-1-one 
• 125741-99-3 2-fluoro-3-hydroxy-1,3-diphenyl-2-(trifluoromethyl)-1-propanone 

Relevant articles and documents

A New Effective and Convenient Route to Fluorinated Nitrogen Heterocyclic Compounds by the Use of Enol Phosphates Derived from F-Alkyl Ketones

The treatment of F-alkyl ketones with sodium diethyl phosphite in tetrahydrofuran at -10 to 0 deg C gave high yields of 1-substituted F-1-alkenyl phosphates, which readily reacted with amidine of hydrazine derivatives at room temperature to afford the cor