71035-25-1

Basic information

• Product Name: 2-Propen-1-one, 1-(4-methoxyphenyl)-3-(4-morpholinyl)-, (E)-
• CAS NO: 71035-25-1
• Molecular Formula: C14H17NO3
• Molecular Weight: 247.294
• Mol File: 71035-25-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 1-(4-methoxyphenyl)-3-(4-morpholinyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 1-(4-methoxyphenyl)-3-(4-morpholinyl)-, (E)-(71035-25-1)
• EPA Substance Registry System: 2-Propen-1-one, 1-(4-methoxyphenyl)-3-(4-morpholinyl)-, (E)-(71035-25-1)

Safety Data

• Hazardous Substances Data: 71035-25-1(Hazardous Substances Data)

Upstream product

• 5770-77-4 1-(4-methoxyphenyl)-3-morpholinopropan-1-one 
• 110-91-8 morpholine 
• 19115-30-1 1-(4-methoxyphenyl)-2-propyn-1-ol 
• 90696-21-2 3-(4-methoxyphenyl)propynal 
• 5349-60-0 1-(4-methoxyphenyl)-1-propanol 
• 121-97-1 4-Methoxypropiophenone 
• 711-33-1 4-trifluoromethyl propiophenone 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 41850-83-3 3-acetoxy-1-(4-methoxy-phenyl)-propenone 

Downstream Products

• 109562-49-4 3-(morpholin-1-yl)-1-(4-methoxyphenyl)propan-1-ol 

Relevant articles and documents

The influence of substituents on the photochemical generation and stability of 2-morpholinocyclopropanols

By irradiation in oxygen-free ether α- or β-substituted β-morpholinopropiophenones 1a-c form the corresponding cyclopropanols 2 with 1-aryl and 2-morpholino group in a relative cis-configuration in high yields. The photocyclization of pure 1a-c enantiomer

Tunable and Diastereoselective Br?nsted Acid Catalyzed Synthesis of β-Enaminones

The Br?nsted acid catalyzed Meyer-Schuster reaction of hemiaminals was studied for the stereoselective synthesis of β-enaminones. Hemiaminals were formed from propargyl aldehydes (or the oxidation of propargyl alcohols) and amines in the presence of Br?ns

Nickel-catalyzed formation of a carbon-nitrogen bond at the β position of saturated ketones

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