25039-19-4

Basic information

• Product Name: (E)-3-morpholino-1-phenyl-2-propen-1-one
• Synonyms: (E)-3-morpholino-1-phenyl-2-propen-1-one
• CAS NO: 25039-19-4
• Molecular Weight: 217.268
• Mol File: 25039-19-4.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: (E)-3-morpholino-1-phenyl-2-propen-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-morpholino-1-phenyl-2-propen-1-one(25039-19-4)
• EPA Substance Registry System: (E)-3-morpholino-1-phenyl-2-propen-1-one(25039-19-4)

Safety Data

• Hazardous Substances Data: 25039-19-4(Hazardous Substances Data)

Upstream product

• 110-91-8 morpholine 
• 2579-22-8 Phenylpropargyl aldehyde 
• 1504-58-1 3-Phenyl-2-propyn-1-ol 
• 4187-87-5 1-Phenyl-2-propyn-1-ol 
• 3623-15-2 phenyl propargyl ketone 
• 93-55-0 1-phenyl-propan-1-one 
• 93-54-9 1-Phenyl-1-propanol 
• 2298-48-8 3-morpholin-4-yl-1-phenyl-propan-1-one 
• 5337-93-9 4'-methylpropiophenone 
• 98-86-2 acetophenone 
• 35534-35-1 morpholino-diethoxy-methane 
• 122-51-0 orthoformic acid triethyl ester 

Downstream Products

• 122438-09-9 (6,8-Dibromo-2-morpholin-4-yl-2H-chromen-3-yl)-phenyl-methanone 
• 120450-91-1 3-benzoyl-4H-chromene 
• 122438-05-5 (6-Fluoro-2-morpholin-4-yl-2H-chromen-3-yl)-phenyl-methanone 
• 122438-08-8 (6-Bromo-8-methoxy-2-morpholin-4-yl-2H-chromen-3-yl)-phenyl-methanone 
• 122438-01-1 (2-Morpholin-4-yl-2H-chromen-3-yl)-phenyl-methanone 
• 122438-03-3 (6-Chloro-2-morpholin-4-yl-2H-chromen-3-yl)-phenyl-methanone 
• 122438-10-2 (3-Morpholin-4-yl-3H-benzo[f]chromen-2-yl)-phenyl-methanone 
• 122438-04-4 (6-Bromo-2-morpholin-4-yl-2H-chromen-3-yl)-phenyl-methanone 
• 2298-48-8 3-morpholin-4-yl-1-phenyl-propan-1-one 
• 4441-34-3 3-morpholino-1-phenylpropan-1-ol 
• 56570-47-9 (Z)-3-(benzylamino)-1-phenylprop-2-en-1-one 
• 34597-73-4 3-(Benzylamino)-1-phenyl-1-propanol 
• 122438-06-6 (2-Morpholin-4-yl-6-nitro-2H-chromen-3-yl)-phenyl-methanone 
• 122438-07-7 (8-Methoxy-2-morpholin-4-yl-2H-chromen-3-yl)-phenyl-methanone 

Relevant articles and documents

Intermolecular Multiple Dehydrogenative Cross-Couplings of Ketones with Boronic Acids and Amines via Copper Catalysis

An efficient and versatile oxidative coupling reaction was developed for the synthesis of valuable β-functionalized unsaturated ketones and meta-substituted phenols. In the case of intramolecular reactions, achieving rapid molecular complexity through multiple dehydrogenative couplings is already a well-established strategy. Herein, we report an intermolecular multiple dehydrogenative coupling between ketones and nucleophilic amines or boronic acids using inexpensive copper(I) oxide as a catalyst. This method provides a facile access to highly desirable chemical products such as α,β-unsaturated ketones, enaminones, and synthetically relevant meta-substituted phenols. (Figure presented.).

Compounds containing N-alpha, beta unsaturated ketone and preparation method and application of compounds

The invention belongs to the technical field of organic synthesis and particularly relates to compounds containing N-alpha, beta unsaturated ketone and a preparation method and application of the compounds. The preparation method includes: dissolving a co

Synthesis of Polyaromatic Rings: Rh(III)-Catalyzed [5 + 1] Annulation of Enaminones with Vinyl Esters through C-H Bond Functionalization

An expedient [5 + 1] annulation method via Rh(III)-catalyzed C-H bond functionalization of enaminones to synthesize polyaromatic rings is described. The reaction tolerates a broad range of functional groups and offers a new entry to construct polycyclic a