148715-54-2

Basic information

• Product Name: 4-<2(E)-(4,5-diphenyl-2-oxo-4-oxazolin-3-yl)ethenyl>phenol
• Synonyms: 4-<2(E)-(4,5-diphenyl-2-oxo-4-oxazolin-3-yl)ethenyl>phenol
• CAS NO: 148715-54-2
• Molecular Weight: 355.393
• Mol File: 148715-54-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-<2(E)-(4,5-diphenyl-2-oxo-4-oxazolin-3-yl)ethenyl>phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-<2(E)-(4,5-diphenyl-2-oxo-4-oxazolin-3-yl)ethenyl>phenol(148715-54-2)
• EPA Substance Registry System: 4-<2(E)-(4,5-diphenyl-2-oxo-4-oxazolin-3-yl)ethenyl>phenol(148715-54-2)

Safety Data

• Hazardous Substances Data: 148715-54-2(Hazardous Substances Data)

Upstream product

• 148715-45-1 3-(2-iodoethyl)-4,5-diphenyl-2(3H)oxazolone 
• 148715-44-0 N-(2-chloroethyl)-4,5-diphenyl-4-oxazolin-2-one 
• 540-38-5 p-Iodophenol 
• 148715-46-2 3-ethenyl-4,5-diphenyl-2(3H)oxazolone 

Downstream Products

• 60-19-5 tyramine hydrochloride 

Relevant articles and documents

Phenethylamines via Heck Arylation of a New Vinylamine Equivalent

A new vinylamine equivalent, N-vinyloxazolone 3, has been prepared in three steps and shown to undergo Heck arylation with a variety of substrates.The Heck adducts thus obtained are then converted in one step and high yield to phenethylamine hydrochlorides.As a general synthetic method for preparation of substituted phenethylamines, use of this new reagent is shown to be superior to N-vinylphthalimide in number of steps, regiospecificity, and chemical yield.