140866-59-7

Basic information

• Product Name: 2-Propen-1-one, 3-(dimethylamino)-1,2-diphenyl-, (E)-
• Synonyms: 3-(dimethylamino)-1,2-diphenyl-2-propen-1-one;3-dimethylamino-1,2-diphenylprop-2-en-1-one;(E)-3-Dimethylamino-1,2-diphenyl-propenone;3-(dimethylamino)-1,2-diphenylprop-2-enone
• CAS NO: 140866-59-7
• Molecular Formula: C17H17NO
• Molecular Weight: 251.32300
• Mol File: 140866-59-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 3-(dimethylamino)-1,2-diphenyl-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 3-(dimethylamino)-1,2-diphenyl-, (E)-(140866-59-7)
• EPA Substance Registry System: 2-Propen-1-one, 3-(dimethylamino)-1,2-diphenyl-, (E)-(140866-59-7)

Safety Data

• Hazardous Substances Data: 140866-59-7(Hazardous Substances Data)

Upstream product

• 451-40-1 phenyl benzyl ketone 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 

Downstream Products

• 143621-07-2 (Z)-3-(Hydroxy-methyl-amino)-1,2-diphenyl-propenone 
• 120046-82-4 ethyl 3,4-diphenylpyrrole-2-carboxylate 
• 120982-78-7 ethyl 4,5-diphenyl-1H-pyrazole-1-acetate 
• 5415-07-6 3-oxo-2,3-diphenyl-propionitrile 
• 25922-93-4 4,5-diphenylpyrimidine 
• 36372-77-7 1,4,5-triphenyl-1H-pyrazole 
• 14677-21-5 (4,5-diphenyl)isoxazole 
• 22563-99-1 3-dimethylamino-1,2-diphenyl-propan-1-one 
• 4452-11-3 1,2-diphenylprop-2-en-1-one 

Relevant articles and documents

Synthesis and photochromism of some mono and bis (thienyl) substituted oxathiine 2,2-dioxides

1,2-Oxathiine 2,2-dioxides have been obtained from their respective 3,4-dihydro-4-dimethylamino precursors, for the first time, by a mild Cope elimination of the 4-dimethylamino function. The application of the 1,2-oxathiine 2,2-dioxide scaffold in materi

A convenient alternative route to β-aminoketones

Enaminones has been prepared and submitted to conjugate reduction with LAH and the system Al2O3/R2NH to give β-aminoketones. The latter tandem amination system has also been applied in the Mannich reaction, improving the synthesis of several new diaryl β-aminoketones. Besides, the sequential use of DMFDMA and LAH-CuI on deoxybenzoins furnishes a new route for the synthesis of enones.